Canonical Allele Identifier: CA1619116533

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354178A= , CM000668.2:g.31354178A=	GRCh38
NC_000006.11:g.31321955A= , CM000668.1:g.31321955A=	GRCh37
NC_000006.10:g.31429934A=	NCBI36
NG_023187.1:g.8035T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3259T=
ENST00000481849.6:n.3219T=
ENST00000497377.6:n.3126T=
ENST00000696558.1:c.1281T=	ENSP00000512716.1:n.1281T=
ENST00000696559.1:c.*123T=	ENSP00000512717.1:n.*123T=
ENST00000696560.1:c.*123T=	ENSP00000512718.1:n.*123T=
ENST00000696561.1:c.*123T=	ENSP00000512719.1:n.*123T=
ENST00000696562.1:c.*123T=	ENSP00000512720.1:n.*123T=
ENST00000412585.7:c.*123T= MANE Select	ENSP00000399168.2:n.*123T=
ENST00000412585.6:c.*123T=	ENSP00000399168.2:n.*123T=
ENST00000481849.5:n.447T=
ENST00000497377.5:n.611T=
NM_005514.6:c.*123T=	NP_005505.2:n.*123T=
XM_011514556.1:c.*123T=	XP_011512858.1:n.*123T=
XM_011514557.1:c.*123T=	XP_011512859.1:n.*123T=
XR_926175.1:n.1651T=
NM_005514.7:c.*123T=	NP_005505.2:n.*123T=
NM_005514.8:c.*123T= MANE Select	NP_005505.2:n.*123T=