Canonical Allele Identifier: CA363311444

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355592-T-C
• MyVariant Identifiers: chr6:g.31323369T>C (hg19) ; chr6:g.31355592T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355592T>C , CM000668.2:g.31355592T>C	GRCh38
NC_000006.11:g.31323369T>C , CM000668.1:g.31323369T>C	GRCh37
NC_000006.10:g.31431348T>C	NCBI36
NG_023187.1:g.6621A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2667A>G
ENST00000481849.6:n.2093A>G
ENST00000497377.6:n.2093A>G
ENST00000640094.2:c.620A>G	ENSP00000491275.2:p.Asp207Gly
ENST00000696558.1:c.689A>G	ENSP00000512716.1:n.689A>G
ENST00000696559.1:c.620A>G	ENSP00000512717.1:p.Asp207Gly
ENST00000696560.1:c.620A>G	ENSP00000512718.1:p.Asp207Gly
ENST00000696561.1:c.620A>G	ENSP00000512719.1:p.Asp207Gly
ENST00000696562.1:c.620A>G	ENSP00000512720.1:p.Asp207Gly
ENST00000412585.7:c.620A>G MANE Select	ENSP00000399168.2:p.Asp207Gly
ENST00000412585.6:c.620A>G	ENSP00000399168.2:p.Asp207Gly
ENST00000434333.1:c.653A>G	ENSP00000405931.1:p.Asp218Gly
ENST00000463574.1:n.211A>G
ENST00000474381.1:n.1069A>G
ENST00000498007.1:n.886A>G
NM_005514.6:c.620A>G	NP_005505.2:p.Asp207Gly
XM_011514556.1:c.653A>G	XP_011512858.1:p.Asp218Gly
XM_011514557.1:c.620A>G	XP_011512859.1:p.Asp207Gly
XR_926175.1:n.1059A>G
NM_005514.7:c.620A>G	NP_005505.2:p.Asp207Gly
NM_005514.8:c.620A>G MANE Select	NP_005505.2:p.Asp207Gly