Canonical Allele Identifier: CA136836446
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs41552212
gnomAD v3: 6-31356738-T-A
gnomAD v4: 6-31356738-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356738T>A , CM000668.2:g.31356738T>A GRCh38
NC_000006.11:g.31324515T>A , CM000668.1:g.31324515T>A GRCh37
NC_000006.10:g.31432494T>A NCBI36
NG_023187.1:g.5475A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1766A>T
ENST00000481849.6:n.1766A>T
ENST00000497377.6:n.1766A>T
ENST00000640094.2:c.293A>T ENSP00000491275.2:p.Asp98Val
ENST00000696558.1:c.293A>T ENSP00000512716.1:p.Asp98Val
ENST00000696559.1:c.293A>T ENSP00000512717.1:p.Asp98Val
ENST00000696560.1:c.293A>T ENSP00000512718.1:p.Asp98Val
ENST00000696561.1:c.293A>T ENSP00000512719.1:p.Asp98Val
ENST00000696562.1:c.293A>T ENSP00000512720.1:p.Asp98Val
ENST00000412585.7:c.293A>T MANE Select ENSP00000399168.2:p.Asp98Val
ENST00000412585.6:c.293A>T ENSP00000399168.2:p.Asp98Val
ENST00000434333.1:c.326A>T ENSP00000405931.1:p.Asp109Val
ENST00000474381.1:n.168A>T
ENST00000498007.1:n.314A>T
ENST00000603274.1:n.92T>A
NM_005514.6:c.293A>T NP_005505.2:p.Asp98Val
XM_011514556.1:c.326A>T XP_011512858.1:p.Asp109Val
XM_011514557.1:c.293A>T XP_011512859.1:p.Asp98Val
XR_926175.1:n.303A>T
NM_005514.7:c.293A>T NP_005505.2:p.Asp98Val
NM_005514.8:c.293A>T MANE Select NP_005505.2:p.Asp98Val