Canonical Allele Identifier: CA449790581

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355425-T-G
• MyVariant Identifiers: chr6:g.31323202T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355425T>G , CM000668.2:g.31355425T>G	GRCh38
NC_000006.11:g.31323202T>G , CM000668.1:g.31323202T>G	GRCh37
NC_000006.10:g.31431181T>G	NCBI36
NG_023187.1:g.6788A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2834A>C
ENST00000481849.6:n.2260A>C
ENST00000497377.6:n.2260A>C
ENST00000640094.2:c.787A>C	ENSP00000491275.2:p.Arg263=
ENST00000696558.1:c.856A>C	ENSP00000512716.1:n.856A>C
ENST00000696559.1:c.787A>C	ENSP00000512717.1:p.Arg263=
ENST00000696560.1:c.787A>C	ENSP00000512718.1:p.Arg263=
ENST00000696561.1:c.787A>C	ENSP00000512719.1:p.Arg263=
ENST00000696562.1:c.787A>C	ENSP00000512720.1:p.Arg263=
ENST00000412585.7:c.787A>C MANE Select	ENSP00000399168.2:p.Arg263=
ENST00000412585.6:c.787A>C	ENSP00000399168.2:p.Arg263=
ENST00000463574.1:n.378A>C
ENST00000498007.1:n.1053A>C
NM_005514.6:c.787A>C	NP_005505.2:p.Arg263=
XM_011514556.1:c.820A>C	XP_011512858.1:p.Arg274=
XM_011514557.1:c.787A>C	XP_011512859.1:p.Arg263=
XR_926175.1:n.1226A>C
NM_005514.7:c.787A>C	NP_005505.2:p.Arg263=
NM_005514.8:c.787A>C MANE Select	NP_005505.2:p.Arg263=