Linked Data
dbSNP Id:
rs2113736277
gnomAD v3:
6-31355267-G-GGCTCCAGAAGC
gnomAD v4:
6-31355267-G-GGCTCCAGAAGC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31355272_31355273insAGAAGCGCTCC , CM000668.2:g.31355272_31355273insAGAAGCGCTCC | GRCh38 |
| NC_000006.11:g.31323049_31323050insAGAAGCGCTCC , CM000668.1:g.31323049_31323050insAGAAGCGCTCC | GRCh37 |
| NC_000006.10:g.31431028_31431029insAGAAGCGCTCC | NCBI36 |
| NG_023187.1:g.6945_6946insGCTTCTGGAGC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000474381.2:n.2943-45_2943-44insGCTTCTGGAGC (HLA-B) | ||
| ENST00000481849.6:n.2417_2418insGCTTCTGGAGC (HLA-B) | ||
| ENST00000497377.6:n.2369-45_2369-44insGCTTCTGGAGC (HLA-B) | ||
| ENST00000640094.2:c.895+49_895+50insGCTTCTGGAGC (HLA-B) | ENSP00000491275.2:n.895+49_895+50insGCTTCTGGAGC | |
| ENST00000696558.1:c.965-45_965-44insGCTTCTGGAGC (HLA-B) | ENSP00000512716.1:n.965-45_965-44insGCTTCTGGAGC | |
| ENST00000696559.1:c.896-45_896-44insGCTTCTGGAGC (HLA-B) | ENSP00000512717.1:n.896-45_896-44insGCTTCTGGAGC | |
| ENST00000696560.1:c.896-45_896-44insGCTTCTGGAGC (HLA-B) | ENSP00000512718.1:n.896-45_896-44insGCTTCTGGAGC | |
| ENST00000696561.1:c.896-45_896-44insGCTTCTGGAGC (HLA-B) | ENSP00000512719.1:n.896-45_896-44insGCTTCTGGAGC | |
| ENST00000696562.1:c.896-45_896-44insGCTTCTGGAGC (HLA-B) | ENSP00000512720.1:n.896-45_896-44insGCTTCTGGAGC | |
| ENST00000412585.7:c.896-45_896-44insGCTTCTGGAGC (HLA-B) MANE Select | ENSP00000399168.2:n.896-45_896-44insGCTTCTGGAGC | |
| ENST00000640094.1:c.88+49_88+50insGCTTCTGGAGC (HLA-B) | ENSP00000491275.1:n.88+49_88+50insGCTTCTGGAGC | |
| ENST00000412585.6:c.896-45_896-44insGCTTCTGGAGC (HLA-B) | ENSP00000399168.2:n.896-45_896-44insGCTTCTGGAGC | |
| ENST00000463574.1:n.487-45_487-44insGCTTCTGGAGC (HLA-B) | ||
| NM_005514.6:c.896-45_896-44insGCTTCTGGAGC (HLA-B) | NP_005505.2:n.896-45_896-44insGCTTCTGGAGC | |
| NR_106951.1:n.49_50insGCTTCTGGAGC (MIR6891) | ||
| XM_011514556.1:c.929-45_929-44insGCTTCTGGAGC (HLA-B) | XP_011512858.1:n.929-45_929-44insGCTTCTGGAGC | |
| XM_011514557.1:c.895+49_895+50insGCTTCTGGAGC (HLA-B) | XP_011512859.1:n.895+49_895+50insGCTTCTGGAGC | |
| XR_926175.1:n.1335-45_1335-44insGCTTCTGGAGC (HLA-B) | ||
| NM_005514.7:c.896-45_896-44insGCTTCTGGAGC (HLA-B) | NP_005505.2:n.896-45_896-44insGCTTCTGGAGC | |
| NM_005514.8:c.896-45_896-44insGCTTCTGGAGC (HLA-B) MANE Select | NP_005505.2:n.896-45_896-44insGCTTCTGGAGC |