Canonical Allele Identifier: CA363312337
Gene: HLA-B HGNC NCBI

Linked Data

gnomAD v3: 6-31356235-A-C
gnomAD v4: 6-31356235-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356235A>C , CM000668.2:g.31356235A>C GRCh38
NC_000006.11:g.31324012A>C , CM000668.1:g.31324012A>C GRCh37
NC_000006.10:g.31431991A>C NCBI36
NG_023187.1:g.5978T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2024T>G
ENST00000481849.6:n.2024T>G
ENST00000497377.6:n.2024T>G
ENST00000640094.2:c.551T>G ENSP00000491275.2:p.Leu184Arg
ENST00000696558.1:c.551T>G ENSP00000512716.1:p.Leu184Arg
ENST00000696559.1:c.551T>G ENSP00000512717.1:p.Leu184Arg
ENST00000696560.1:c.551T>G ENSP00000512718.1:p.Leu184Arg
ENST00000696561.1:c.551T>G ENSP00000512719.1:p.Leu184Arg
ENST00000696562.1:c.551T>G ENSP00000512720.1:p.Leu184Arg
ENST00000412585.7:c.551T>G MANE Select ENSP00000399168.2:p.Leu184Arg
ENST00000412585.6:c.551T>G ENSP00000399168.2:p.Leu184Arg
ENST00000434333.1:c.584T>G ENSP00000405931.1:p.Leu195Arg
ENST00000474381.1:n.426T>G
ENST00000498007.1:n.817T>G
NM_005514.6:c.551T>G NP_005505.2:p.Leu184Arg
XM_011514556.1:c.584T>G XP_011512858.1:p.Leu195Arg
XM_011514557.1:c.551T>G XP_011512859.1:p.Leu184Arg
XR_926175.1:n.561T>G
NM_005514.7:c.551T>G NP_005505.2:p.Leu184Arg
NM_005514.8:c.551T>G MANE Select NP_005505.2:p.Leu184Arg