Linked Data
dbSNP Id:
rs368161759
ExAC:
6:31323048 C / CCAGAAGGG
gnomAD v2:
6-31323048-C-CCAGAAGGG
gnomAD v3:
6-31355271-C-CCAGAAGGG
gnomAD v4:
6-31355271-C-CCAGAAGGG
MyVariant Identifiers:
chr6:g.31323048_31323049insCAGAAGGG (hg19)
chr6:g.31355271_31355272insCAGAAGGG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31355272_31355273insAGAAGGGC , CM000668.2:g.31355272_31355273insAGAAGGGC | GRCh38 |
| NC_000006.11:g.31323049_31323050insAGAAGGGC , CM000668.1:g.31323049_31323050insAGAAGGGC | GRCh37 |
| NC_000006.10:g.31431028_31431029insAGAAGGGC | NCBI36 |
| NG_023187.1:g.6941_6942insCCCTTCTG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000474381.2:n.2942+45_2942+46insCCCTTCTG (HLA-B) | ||
| ENST00000481849.6:n.2413_2414insCCCTTCTG (HLA-B) | ||
| ENST00000497377.6:n.2368+45_2368+46insCCCTTCTG (HLA-B) | ||
| ENST00000640094.2:c.895+45_895+46insCCCTTCTG (HLA-B) | ENSP00000491275.2:n.895+45_895+46insCCCTTCTG | |
| ENST00000696558.1:c.964+45_964+46insCCCTTCTG (HLA-B) | ENSP00000512716.1:n.964+45_964+46insCCCTTCTG | |
| ENST00000696559.1:c.895+45_895+46insCCCTTCTG (HLA-B) | ENSP00000512717.1:n.895+45_895+46insCCCTTCTG | |
| ENST00000696560.1:c.895+45_895+46insCCCTTCTG (HLA-B) | ENSP00000512718.1:n.895+45_895+46insCCCTTCTG | |
| ENST00000696561.1:c.895+45_895+46insCCCTTCTG (HLA-B) | ENSP00000512719.1:n.895+45_895+46insCCCTTCTG | |
| ENST00000696562.1:c.895+45_895+46insCCCTTCTG (HLA-B) | ENSP00000512720.1:n.895+45_895+46insCCCTTCTG | |
| ENST00000412585.7:c.895+45_895+46insCCCTTCTG (HLA-B) MANE Select | ENSP00000399168.2:n.895+45_895+46insCCCTTCTG | |
| ENST00000640094.1:c.88+45_88+46insCCCTTCTG (HLA-B) | ENSP00000491275.1:n.88+45_88+46insCCCTTCTG | |
| ENST00000412585.6:c.895+45_895+46insCCCTTCTG (HLA-B) | ENSP00000399168.2:n.895+45_895+46insCCCTTCTG | |
| ENST00000463574.1:n.486+45_486+46insCCCTTCTG (HLA-B) | ||
| NM_005514.6:c.895+45_895+46insCCCTTCTG (HLA-B) | NP_005505.2:n.895+45_895+46insCCCTTCTG | |
| NR_106951.1:n.45_46insCCCTTCTG (MIR6891) | ||
| XM_011514556.1:c.928+45_928+46insCCCTTCTG (HLA-B) | XP_011512858.1:n.928+45_928+46insCCCTTCTG | |
| XM_011514557.1:c.895+45_895+46insCCCTTCTG (HLA-B) | XP_011512859.1:n.895+45_895+46insCCCTTCTG | |
| XR_926175.1:n.1334+45_1334+46insCCCTTCTG (HLA-B) | ||
| NM_005514.7:c.895+45_895+46insCCCTTCTG (HLA-B) | NP_005505.2:n.895+45_895+46insCCCTTCTG | |
| NM_005514.8:c.895+45_895+46insCCCTTCTG (HLA-B) MANE Select | NP_005505.2:n.895+45_895+46insCCCTTCTG |