Canonical Allele Identifier: CA449599575

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31354504-A-C
• gnomAD v4: 6-31354504-A-C
• MyVariant Identifiers: chr6:g.31322281A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354504A>C , CM000668.2:g.31354504A>C	GRCh38
NC_000006.11:g.31322281A>C , CM000668.1:g.31322281A>C	GRCh37
NC_000006.10:g.31430260A>C	NCBI36
NG_023187.1:g.7709T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3115T>G
ENST00000481849.6:n.3075T>G
ENST00000497377.6:n.2982T>G
ENST00000640094.2:c.951T>G	ENSP00000491275.2:p.Ser317=
ENST00000696558.1:c.1137T>G	ENSP00000512716.1:n.1137T>G
ENST00000696559.1:c.1068T>G	ENSP00000512717.1:p.Ser356=
ENST00000696560.1:c.1068T>G	ENSP00000512718.1:p.Ser356=
ENST00000696561.1:c.1068T>G	ENSP00000512719.1:p.Ser356=
ENST00000696562.1:c.1068T>G	ENSP00000512720.1:p.Ser356=
ENST00000412585.7:c.1068T>G MANE Select	ENSP00000399168.2:p.Ser356=
ENST00000640094.1:c.144T>G	ENSP00000491275.1:p.Ser48=
ENST00000412585.6:c.1068T>G	ENSP00000399168.2:p.Ser356=
ENST00000481849.5:n.303T>G
ENST00000497377.5:n.467T>G
NM_005514.6:c.1068T>G	NP_005505.2:p.Ser356=
XM_011514556.1:c.1101T>G	XP_011512858.1:p.Ser367=
XM_011514557.1:c.951T>G	XP_011512859.1:p.Ser317=
XR_926175.1:n.1507T>G
NM_005514.7:c.1068T>G	NP_005505.2:p.Ser356=
NM_005514.8:c.1068T>G MANE Select	NP_005505.2:p.Ser356=