Canonical Allele Identifier: CA363307979

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354516-A-C
• MyVariant Identifiers: chr6:g.31322293A>C (hg19) ; chr6:g.31354516A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354516A>C , CM000668.2:g.31354516A>C	GRCh38
NC_000006.11:g.31322293A>C , CM000668.1:g.31322293A>C	GRCh37
NC_000006.10:g.31430272A>C	NCBI36
NG_023187.1:g.7697T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3103T>G
ENST00000481849.6:n.3063T>G
ENST00000497377.6:n.2970T>G
ENST00000640094.2:c.939T>G	ENSP00000491275.2:p.Ser313Arg
ENST00000696558.1:c.1125T>G	ENSP00000512716.1:n.1125T>G
ENST00000696559.1:c.1056T>G	ENSP00000512717.1:p.Ser352Arg
ENST00000696560.1:c.1056T>G	ENSP00000512718.1:p.Ser352Arg
ENST00000696561.1:c.1056T>G	ENSP00000512719.1:p.Ser352Arg
ENST00000696562.1:c.1056T>G	ENSP00000512720.1:p.Ser352Arg
ENST00000412585.7:c.1056T>G MANE Select	ENSP00000399168.2:p.Ser352Arg
ENST00000640094.1:c.132T>G	ENSP00000491275.1:p.Ser44Arg
ENST00000412585.6:c.1056T>G	ENSP00000399168.2:p.Ser352Arg
ENST00000481849.5:n.291T>G
ENST00000497377.5:n.455T>G
NM_005514.6:c.1056T>G	NP_005505.2:p.Ser352Arg
XM_011514556.1:c.1089T>G	XP_011512858.1:p.Ser363Arg
XM_011514557.1:c.939T>G	XP_011512859.1:p.Ser313Arg
XR_926175.1:n.1495T>G
NM_005514.7:c.1056T>G	NP_005505.2:p.Ser352Arg
NM_005514.8:c.1056T>G MANE Select	NP_005505.2:p.Ser352Arg