Canonical Allele Identifier: CA1619117222

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354502T= , CM000668.2:g.31354502T=	GRCh38
NC_000006.11:g.31322279T= , CM000668.1:g.31322279T=	GRCh37
NC_000006.10:g.31430258T=	NCBI36
NG_023187.1:g.7711A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3117A=
ENST00000481849.6:n.3077A=
ENST00000497377.6:n.2984A=
ENST00000640094.2:c.953A=	ENSP00000491275.2:p.Asp318=
ENST00000696558.1:c.1139A=	ENSP00000512716.1:n.1139A=
ENST00000696559.1:c.1070A=	ENSP00000512717.1:p.Asp357=
ENST00000696560.1:c.1070A=	ENSP00000512718.1:p.Asp357=
ENST00000696561.1:c.1070A=	ENSP00000512719.1:p.Asp357=
ENST00000696562.1:c.1070A=	ENSP00000512720.1:p.Asp357=
ENST00000412585.7:c.1070A= MANE Select	ENSP00000399168.2:p.Asp357=
ENST00000640094.1:c.146A=	ENSP00000491275.1:p.Asp49=
ENST00000412585.6:c.1070A=	ENSP00000399168.2:p.Asp357=
ENST00000481849.5:n.305A=
ENST00000497377.5:n.469A=
NM_005514.6:c.1070A=	NP_005505.2:p.Asp357=
XM_011514556.1:c.1103A=	XP_011512858.1:p.Asp368=
XM_011514557.1:c.953A=	XP_011512859.1:p.Asp318=
XR_926175.1:n.1509A=
NM_005514.7:c.1070A=	NP_005505.2:p.Asp357=
NM_005514.8:c.1070A= MANE Select	NP_005505.2:p.Asp357=