Canonical Allele Identifier: CA3711813
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs151341152
gnomAD v3: 6-31356804-A-C
gnomAD v4: 6-31356804-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356804A>C , CM000668.2:g.31356804A>C GRCh38
NC_000006.11:g.31324581A>C , CM000668.1:g.31324581A>C GRCh37
NC_000006.10:g.31432560A>C NCBI36
NG_023187.1:g.5409T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1700T>G
ENST00000481849.6:n.1700T>G
ENST00000497377.6:n.1700T>G
ENST00000640094.2:c.227T>G ENSP00000491275.2:p.Ile76Arg
ENST00000696558.1:c.227T>G ENSP00000512716.1:p.Ile76Arg
ENST00000696559.1:c.227T>G ENSP00000512717.1:p.Ile76Arg
ENST00000696560.1:c.227T>G ENSP00000512718.1:p.Ile76Arg
ENST00000696561.1:c.227T>G ENSP00000512719.1:p.Ile76Arg
ENST00000696562.1:c.227T>G ENSP00000512720.1:p.Ile76Arg
ENST00000412585.7:c.227T>G MANE Select ENSP00000399168.2:p.Ile76Arg
ENST00000412585.6:c.227T>G ENSP00000399168.2:p.Ile76Arg
ENST00000434333.1:c.260T>G ENSP00000405931.1:p.Ile87Arg
ENST00000474381.1:n.102T>G
ENST00000498007.1:n.248T>G
ENST00000603274.1:n.158A>C
NM_005514.6:c.227T>G NP_005505.2:p.Ile76Arg
XM_011514556.1:c.260T>G XP_011512858.1:p.Ile87Arg
XM_011514557.1:c.227T>G XP_011512859.1:p.Ile76Arg
XR_926175.1:n.237T>G
NM_005514.7:c.227T>G NP_005505.2:p.Ile76Arg
NM_005514.8:c.227T>G MANE Select NP_005505.2:p.Ile76Arg