Canonical Allele Identifier: CA1619119111

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355560T= , CM000668.2:g.31355560T=	GRCh38
NC_000006.11:g.31323337T= , CM000668.1:g.31323337T=	GRCh37
NC_000006.10:g.31431316T=	NCBI36
NG_023187.1:g.6653A=

Transcript Alleles

HGVS	Amino-acid Change
NM_005514.8:c.652A= MANE Select	NP_005505.2:p.Ile218=
ENST00000412585.7:c.652A= MANE Select	ENSP00000399168.2:p.Ile218=
NM_005514.6:c.652A=	NP_005505.2:p.Ile218=
NM_005514.7:c.652A=	NP_005505.2:p.Ile218=
ENST00000412585.6:c.652A=	ENSP00000399168.2:p.Ile218=
ENST00000434333.1:c.685A=	ENSP00000405931.1:p.Ile229=
ENST00000463574.1:n.243A=
ENST00000474381.1:n.1101A=
ENST00000474381.2:n.2699A=
ENST00000481849.6:n.2125A=
ENST00000497377.6:n.2125A=
ENST00000498007.1:n.918A=
ENST00000640094.2:c.652A=	ENSP00000491275.2:p.Ile218=
ENST00000696558.1:c.721A=	ENSP00000512716.1:n.721A=
ENST00000696559.1:c.652A=	ENSP00000512717.1:p.Ile218=
ENST00000696560.1:c.652A=	ENSP00000512718.1:p.Ile218=
ENST00000696561.1:c.652A=	ENSP00000512719.1:p.Ile218=
ENST00000696562.1:c.652A=	ENSP00000512720.1:p.Ile218=
XM_011514556.1:c.685A=	XP_011512858.1:p.Ile229=
XM_011514557.1:c.652A=	XP_011512859.1:p.Ile218=
XR_926175.1:n.1091A=