Linked Data
dbSNP Id:
rs1562163667
gnomAD v2:
6-31323049-C-CAGAAGGGCTCT
gnomAD v4:
6-31355272-C-CAGAAGGGCTCT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31355272_31355273insAGAAGGGCTCT , CM000668.2:g.31355272_31355273insAGAAGGGCTCT | GRCh38 |
| NC_000006.11:g.31323049_31323050insAGAAGGGCTCT , CM000668.1:g.31323049_31323050insAGAAGGGCTCT | GRCh37 |
| NC_000006.10:g.31431028_31431029insAGAAGGGCTCT | NCBI36 |
| NG_023187.1:g.6940_6941insAGAGCCCTTCT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000474381.2:n.2942+44_2942+45insAGAGCCCTTCT (HLA-B) | ||
| ENST00000481849.6:n.2412_2413insAGAGCCCTTCT (HLA-B) | ||
| ENST00000497377.6:n.2368+44_2368+45insAGAGCCCTTCT (HLA-B) | ||
| ENST00000640094.2:c.895+44_895+45insAGAGCCCTTCT (HLA-B) | ENSP00000491275.2:n.895+44_895+45insAGAGCCCTTCT | |
| ENST00000696558.1:c.964+44_964+45insAGAGCCCTTCT (HLA-B) | ENSP00000512716.1:n.964+44_964+45insAGAGCCCTTCT | |
| ENST00000696559.1:c.895+44_895+45insAGAGCCCTTCT (HLA-B) | ENSP00000512717.1:n.895+44_895+45insAGAGCCCTTCT | |
| ENST00000696560.1:c.895+44_895+45insAGAGCCCTTCT (HLA-B) | ENSP00000512718.1:n.895+44_895+45insAGAGCCCTTCT | |
| ENST00000696561.1:c.895+44_895+45insAGAGCCCTTCT (HLA-B) | ENSP00000512719.1:n.895+44_895+45insAGAGCCCTTCT | |
| ENST00000696562.1:c.895+44_895+45insAGAGCCCTTCT (HLA-B) | ENSP00000512720.1:n.895+44_895+45insAGAGCCCTTCT | |
| ENST00000412585.7:c.895+44_895+45insAGAGCCCTTCT (HLA-B) MANE Select | ENSP00000399168.2:n.895+44_895+45insAGAGCCCTTCT | |
| ENST00000640094.1:c.88+44_88+45insAGAGCCCTTCT (HLA-B) | ENSP00000491275.1:n.88+44_88+45insAGAGCCCTTCT | |
| ENST00000412585.6:c.895+44_895+45insAGAGCCCTTCT (HLA-B) | ENSP00000399168.2:n.895+44_895+45insAGAGCCCTTCT | |
| ENST00000463574.1:n.486+44_486+45insAGAGCCCTTCT (HLA-B) | ||
| NM_005514.6:c.895+44_895+45insAGAGCCCTTCT (HLA-B) | NP_005505.2:n.895+44_895+45insAGAGCCCTTCT | |
| NR_106951.1:n.44_45insAGAGCCCTTCT (MIR6891) | ||
| XM_011514556.1:c.928+44_928+45insAGAGCCCTTCT (HLA-B) | XP_011512858.1:n.928+44_928+45insAGAGCCCTTCT | |
| XM_011514557.1:c.895+44_895+45insAGAGCCCTTCT (HLA-B) | XP_011512859.1:n.895+44_895+45insAGAGCCCTTCT | |
| XR_926175.1:n.1334+44_1334+45insAGAGCCCTTCT (HLA-B) | ||
| NM_005514.7:c.895+44_895+45insAGAGCCCTTCT (HLA-B) | NP_005505.2:n.895+44_895+45insAGAGCCCTTCT | |
| NM_005514.8:c.895+44_895+45insAGAGCCCTTCT (HLA-B) MANE Select | NP_005505.2:n.895+44_895+45insAGAGCCCTTCT |