Canonical Allele Identifier: CA1619116371

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31353976T= , CM000668.2:g.31353976T=	GRCh38
NC_000006.11:g.31321753T= , CM000668.1:g.31321753T=	GRCh37
NC_000006.10:g.31429732T=	NCBI36
NG_023187.1:g.8237A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3461A=
ENST00000481849.6:n.3421A=
ENST00000497377.6:n.3328A=
ENST00000696558.1:c.1483A=	ENSP00000512716.1:n.1483A=
ENST00000696559.1:c.*325A=	ENSP00000512717.1:n.*325A=
ENST00000696560.1:c.*325A=	ENSP00000512718.1:n.*325A=
ENST00000696561.1:c.*325A=	ENSP00000512719.1:n.*325A=
ENST00000696562.1:c.*325A=	ENSP00000512720.1:n.*325A=
ENST00000412585.7:c.*325A= MANE Select	ENSP00000399168.2:n.*325A=
ENST00000412585.6:c.*325A=	ENSP00000399168.2:n.*325A=
ENST00000481849.5:n.649A=
ENST00000497377.5:n.813A=
NM_005514.6:c.*325A=	NP_005505.2:n.*325A=
XM_011514556.1:c.*325A=	XP_011512858.1:n.*325A=
XM_011514557.1:c.*325A=	XP_011512859.1:n.*325A=
XR_926175.1:n.1853A=
NM_005514.7:c.*325A=	NP_005505.2:n.*325A=
NM_005514.8:c.*325A= MANE Select	NP_005505.2:n.*325A=