Canonical Allele Identifier: CA1619119003

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355500T= , CM000668.2:g.31355500T=	GRCh38
NC_000006.11:g.31323277T= , CM000668.1:g.31323277T=	GRCh37
NC_000006.10:g.31431256T=	NCBI36
NG_023187.1:g.6713A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2759A=
ENST00000481849.6:n.2185A=
ENST00000497377.6:n.2185A=
ENST00000640094.2:c.712A=	ENSP00000491275.2:p.Thr238=
ENST00000696558.1:c.781A=	ENSP00000512716.1:n.781A=
ENST00000696559.1:c.712A=	ENSP00000512717.1:p.Thr238=
ENST00000696560.1:c.712A=	ENSP00000512718.1:p.Thr238=
ENST00000696561.1:c.712A=	ENSP00000512719.1:p.Thr238=
ENST00000696562.1:c.712A=	ENSP00000512720.1:p.Thr238=
ENST00000412585.7:c.712A= MANE Select	ENSP00000399168.2:p.Thr238=
ENST00000412585.6:c.712A=	ENSP00000399168.2:p.Thr238=
ENST00000463574.1:n.303A=
ENST00000498007.1:n.978A=
NM_005514.6:c.712A=	NP_005505.2:p.Thr238=
XM_011514556.1:c.745A=	XP_011512858.1:p.Thr249=
XM_011514557.1:c.712A=	XP_011512859.1:p.Thr238=
XR_926175.1:n.1151A=
NM_005514.7:c.712A=	NP_005505.2:p.Thr238=
NM_005514.8:c.712A= MANE Select	NP_005505.2:p.Thr238=