Canonical Allele Identifier: CA449599698

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354664-A-T
• MyVariant Identifiers: chr6:g.31322441A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354664A>T , CM000668.2:g.31354664A>T	GRCh38
NC_000006.11:g.31322441A>T , CM000668.1:g.31322441A>T	GRCh37
NC_000006.10:g.31430420A>T	NCBI36
NG_023187.1:g.7549T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3061T>A
ENST00000481849.6:n.3021T>A
ENST00000497377.6:n.2928T>A
ENST00000640094.2:c.897T>A	ENSP00000491275.2:p.Gly299=
ENST00000696558.1:c.1083T>A	ENSP00000512716.1:n.1083T>A
ENST00000696559.1:c.1014T>A	ENSP00000512717.1:p.Gly338=
ENST00000696560.1:c.1014T>A	ENSP00000512718.1:p.Gly338=
ENST00000696561.1:c.1014T>A	ENSP00000512719.1:p.Gly338=
ENST00000696562.1:c.1014T>A	ENSP00000512720.1:p.Gly338=
ENST00000412585.7:c.1014T>A MANE Select	ENSP00000399168.2:p.Gly338=
ENST00000640094.1:c.90T>A	ENSP00000491275.1:p.Gly30=
ENST00000412585.6:c.1014T>A	ENSP00000399168.2:p.Gly338=
ENST00000481849.5:n.143T>A
ENST00000497377.5:n.413T>A
NM_005514.6:c.1014T>A	NP_005505.2:p.Gly338=
XM_011514556.1:c.1047T>A	XP_011512858.1:p.Gly349=
XM_011514557.1:c.897T>A	XP_011512859.1:p.Gly299=
XR_926175.1:n.1453T>A
NM_005514.7:c.1014T>A	NP_005505.2:p.Gly338=
NM_005514.8:c.1014T>A MANE Select	NP_005505.2:p.Gly338=