Gene
|
Epitope sequence
|
Genotype of epitope
| |
Class A- Alleles
|
Class B- Alleles
|
---|
| | |
Supertypes
|
A01
|
A02
|
A24
|
A01A03
|
A01A24
|
B07
|
B58
|
B27
|
---|
| | |
Allele type
|
A*01:01
|
A*02:01
|
A*68:02
|
A*23:01
|
A*30:01
|
A*29:02
|
B*07:02
|
B*35:01
|
B*53:01
|
B*57:01
|
B*58:01
|
B*15:03
|
B*27:05
|
---|
NS3 (A*02)
|
CINGVCWTV
|
1a
| |
17802
|
67
|
61
|
14908
|
15501
|
12611
|
23637
|
20927
|
25523
|
19827
|
13679
|
19257
|
23485
|
1073-1081
|
CVNGVCWTV
|
1b
| |
16997
|
110
|
20
|
12228
|
13122
|
11766
|
21885
|
15696
|
13382
|
18288
|
12132
|
20367
|
23007
|
|
SISGVLWTV
|
2a variant
| |
18961
|
11
|
16
|
21483
|
11417
|
11417
|
22455
|
22186
|
29702
|
18590
|
15055
|
15691
|
20667
|
|
TVGGVMWTV
|
3a
| |
19940
|
64
|
8
|
12677
|
14750
|
9776
|
20729
|
21877
|
24623
|
16182
|
18054
|
26500
|
24303
|
|
AVNGVMWTV
|
4a variant
| |
17734
|
23
|
14
|
24001
|
4015#
|
12036
|
10753
|
20258
|
20595
|
17093
|
12996
|
13641
|
18882
|
|
CINGVLWTV
|
5a
| |
15172
|
26
|
39
|
17548
|
13613
|
13865
|
23524
|
21854
|
15854
|
18628
|
11203
|
17516
|
21090
|
|
CINGVMWTL
|
5a variant
| |
17922
|
140
|
101
|
10449
|
14413
|
11435
|
18947
|
13165
|
11237
|
2239
|
13165
|
13572
|
19956
|
NS3 (A*02)
|
KLVALGINA
|
1a
| |
22719
|
273
|
15048
|
32261
|
1830
|
18800
|
24242
|
25216
|
37253
|
23529
|
20557
|
4839
|
19019
|
1406-1415
|
KLSGLGLNA
|
1b
| |
19133
|
475
|
21824
|
33559
|
2557
|
13152
|
20740
|
27147
|
37083
|
23891
|
19220
|
8973
|
18099
|
|
QLTSLGLNA
|
4a
| |
20013
|
7051
|
15292
|
33674
|
12859
|
12517
|
26454
|
24440
|
37244
|
22168
|
26218
|
7165
|
19904
|
|
KLVALGINAV
|
1a
| |
37929
|
52
|
8564
|
39134
|
NO VALUE
|
31977
|
19547
|
42247
|
34339
|
NO VALUE
|
NO VALUE
|
NO VALUE
|
26021
|
|
LTGLGINAV
|
5a
| |
12100
|
5692
|
304
|
32426
|
10980
|
20519
|
21309
|
20981
|
33652
|
25012
|
21599
|
12577
|
26332
|
|
QLTGLGINA
|
5a variant
| |
22408
|
6972
|
7419
|
34672
|
13389
|
17488
|
26117
|
23541
|
36968
|
25569
|
22283
|
15466
|
20054
|
NS4B (A*02)
|
LLFNILGGW
|
1a, 1b, 4, 5a
| |
22942
|
14359
|
17095
|
18086
|
17906
|
9175
|
24903
|
19854
|
17154
|
956#
|
962#
|
5918
|
23118
|
1807-1816
|
MFFNILGGWV
|
3a
| |
24613
|
23482
|
19706
|
343
|
15640
|
1707#
|
21757
|
11817
|
8151
|
10769
|
1251
|
13832
|
26621
|
|
LLFNILGGWV
|
1a, 1b, 4, 5a
| |
32231
|
44
|
1159#
|
38969
|
NO VALUE
|
19453
|
32445
|
40287
|
25767
|
NO VALUE
|
NO VALUE
|
NO VALUE
|
25868
|
NS4B (A*02)
|
ILAGYGAGV
|
1a, 1b, 5a
| |
20500
|
15
|
530#
|
30882
|
15492
|
10120
|
11883
|
21134
|
37213
|
22934
|
20702
|
3735
|
20143
|
1851-1859
|
ILAGYGTGV
|
5a variant
| |
20351
|
18
|
193
|
32028
|
17493
|
12563
|
11272
|
21994
|
36657
|
23555
|
20603
|
2196
|
19849
|
NS5B (B*15)
|
MSYSWTGAL
|
1a, 1b, 4
| |
12612
|
1522
|
24
|
2924
|
2372
|
5457
|
1530#
|
50
|
8456
|
10166
|
523#
|
80
|
16876
|
2422-2433
|
MSYTWTGAL
|
5a
| |
12133
|
2640
|
22
|
8602
|
2141#
|
7606
|
2515#
|
58
|
9150
|
10680
|
787#
|
144
|
17267
|
|
YTWTGALIT
|
5a variant
| |
15779
|
3000
|
13286
|
33166
|
13737
|
1561
|
18979
|
3920
|
27619
|
22480
|
17360
|
6553
|
18765
|
NS5B (A*02)
|
GLQDCTMLV
|
1a
| |
18371
|
8
|
5733
|
11972
|
13187
|
6275
|
20996
|
27015
|
35681
|
25282
|
22002
|
10687
|
17601
|
2727-2735
|
KLQDCTMLV
|
1b
| |
17735
|
7
|
3878
|
6160
|
2071#
|
9527
|
17308
|
26776
|
35038
|
23310
|
18296
|
3587
|
16634
|
|
KLRDCTLLV
|
5a
| |
19744
|
13
|
14912
|
15150
|
10
|
5150
|
2800
|
27145
|
36627
|
21481
|
20362
|
1720#
|
18071
|
|
ALRDCTMLV
|
4a
| |
19976
|
19
|
4673
|
19836
|
29
|
9982
|
5384
|
26302
|
36740
|
24190
|
22343
|
1206#
|
20027
|
- <50 IC50nm, bold, high affinity.
- >50 IC50nm, <500 IC50nm, italic, intermediate affinity.
- >500 IC50nm, #, poor affinity.
- No value indicates server produced no binding score.