Canonical Allele Identifier: CA1619119155

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355576G= , CM000668.2:g.31355576G=	GRCh38
NC_000006.11:g.31323353G= , CM000668.1:g.31323353G=	GRCh37
NC_000006.10:g.31431332G=	NCBI36
NG_023187.1:g.6637C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2683C=
ENST00000481849.6:n.2109C=
ENST00000497377.6:n.2109C=
ENST00000640094.2:c.636C=	ENSP00000491275.2:p.His212=
ENST00000696558.1:c.705C=	ENSP00000512716.1:n.705C=
ENST00000696559.1:c.636C=	ENSP00000512717.1:p.His212=
ENST00000696560.1:c.636C=	ENSP00000512718.1:p.His212=
ENST00000696561.1:c.636C=	ENSP00000512719.1:p.His212=
ENST00000696562.1:c.636C=	ENSP00000512720.1:p.His212=
ENST00000412585.7:c.636C= MANE Select	ENSP00000399168.2:p.His212=
ENST00000412585.6:c.636C=	ENSP00000399168.2:p.His212=
ENST00000434333.1:c.669C=	ENSP00000405931.1:p.His223=
ENST00000463574.1:n.227C=
ENST00000474381.1:n.1085C=
ENST00000498007.1:n.902C=
NM_005514.6:c.636C=	NP_005505.2:p.His212=
XM_011514556.1:c.669C=	XP_011512858.1:p.His223=
XM_011514557.1:c.636C=	XP_011512859.1:p.His212=
XR_926175.1:n.1075C=
NM_005514.7:c.636C=	NP_005505.2:p.His212=
NM_005514.8:c.636C= MANE Select	NP_005505.2:p.His212=