Canonical Allele Identifier: CA1619114355

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357146C= , CM000668.2:g.31357146C=	GRCh38
NC_000006.11:g.31324923C= , CM000668.1:g.31324923C=	GRCh37
NC_000006.10:g.31432902C=	NCBI36
NG_023187.1:g.5067G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1486G=
ENST00000481849.6:n.1486G=
ENST00000497377.6:n.1486G=
ENST00000640094.2:c.13G=	ENSP00000491275.2:p.Ala5=
ENST00000696558.1:c.13G=	ENSP00000512716.1:p.Ala5=
ENST00000696559.1:c.13G=	ENSP00000512717.1:p.Ala5=
ENST00000696560.1:c.13G=	ENSP00000512718.1:p.Ala5=
ENST00000696561.1:c.13G=	ENSP00000512719.1:p.Ala5=
ENST00000696562.1:c.13G=	ENSP00000512720.1:p.Ala5=
ENST00000412585.7:c.13G= MANE Select	ENSP00000399168.2:p.Ala5=
ENST00000412585.6:c.13G=	ENSP00000399168.2:p.Ala5=
ENST00000434333.1:c.-83G=	ENSP00000405931.1:n.-83G=
ENST00000498007.1:n.34G=
ENST00000603274.1:n.500C=
NM_005514.6:c.13G=	NP_005505.2:p.Ala5=
XM_011514557.1:c.13G=	XP_011512859.1:p.Ala5=
XR_926175.1:n.23G=
NM_005514.7:c.13G=	NP_005505.2:p.Ala5=
NM_005514.8:c.13G= MANE Select	NP_005505.2:p.Ala5=