Canonical Allele Identifier: CA1619116398

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354013G= , CM000668.2:g.31354013G=	GRCh38
NC_000006.11:g.31321790G= , CM000668.1:g.31321790G=	GRCh37
NC_000006.10:g.31429769G=	NCBI36
NG_023187.1:g.8200C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3424C=
ENST00000481849.6:n.3384C=
ENST00000497377.6:n.3291C=
ENST00000696558.1:c.1446C=	ENSP00000512716.1:n.1446C=
ENST00000696559.1:c.*288C=	ENSP00000512717.1:n.*288C=
ENST00000696560.1:c.*288C=	ENSP00000512718.1:n.*288C=
ENST00000696561.1:c.*288C=	ENSP00000512719.1:n.*288C=
ENST00000696562.1:c.*288C=	ENSP00000512720.1:n.*288C=
ENST00000412585.7:c.*288C= MANE Select	ENSP00000399168.2:n.*288C=
ENST00000412585.6:c.*288C=	ENSP00000399168.2:n.*288C=
ENST00000481849.5:n.612C=
ENST00000497377.5:n.776C=
NM_005514.6:c.*288C=	NP_005505.2:n.*288C=
XM_011514556.1:c.*288C=	XP_011512858.1:n.*288C=
XM_011514557.1:c.*288C=	XP_011512859.1:n.*288C=
XR_926175.1:n.1816C=
NM_005514.7:c.*288C=	NP_005505.2:n.*288C=
NM_005514.8:c.*288C= MANE Select	NP_005505.2:n.*288C=