Canonical Allele Identifier: CA3711823
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs151341127
gnomAD v3: 6-31356817-G-A
gnomAD v4: 6-31356817-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356817G>A , CM000668.2:g.31356817G>A GRCh38
NC_000006.11:g.31324594G>A , CM000668.1:g.31324594G>A GRCh37
NC_000006.10:g.31432573G>A NCBI36
NG_023187.1:g.5396C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1687C>T
ENST00000481849.6:n.1687C>T
ENST00000497377.6:n.1687C>T
ENST00000640094.2:c.214C>T ENSP00000491275.2:p.Arg72Trp
ENST00000696558.1:c.214C>T ENSP00000512716.1:p.Arg72Trp
ENST00000696559.1:c.214C>T ENSP00000512717.1:p.Arg72Trp
ENST00000696560.1:c.214C>T ENSP00000512718.1:p.Arg72Trp
ENST00000696561.1:c.214C>T ENSP00000512719.1:p.Arg72Trp
ENST00000696562.1:c.214C>T ENSP00000512720.1:p.Arg72Trp
ENST00000412585.7:c.214C>T MANE Select ENSP00000399168.2:p.Arg72Trp
ENST00000412585.6:c.214C>T ENSP00000399168.2:p.Arg72Trp
ENST00000434333.1:c.247C>T ENSP00000405931.1:p.Arg83Trp
ENST00000474381.1:n.89C>T
ENST00000498007.1:n.235C>T
ENST00000603274.1:n.171G>A
NM_005514.6:c.214C>T NP_005505.2:p.Arg72Trp
XM_011514556.1:c.247C>T XP_011512858.1:p.Arg83Trp
XM_011514557.1:c.214C>T XP_011512859.1:p.Arg72Trp
XR_926175.1:n.224C>T
NM_005514.7:c.214C>T NP_005505.2:p.Arg72Trp
NM_005514.8:c.214C>T MANE Select NP_005505.2:p.Arg72Trp