Canonical Allele Identifier: CA3711354

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355426A>G , CM000668.2:g.31355426A>G	GRCh38
NC_000006.11:g.31323203A>G , CM000668.1:g.31323203A>G	GRCh37
NC_000006.10:g.31431182A>G	NCBI36
NG_023187.1:g.6787T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_005514.8:c.786T>C MANE Select	NP_005505.2:p.Asp262=
ENST00000412585.7:c.786T>C MANE Select	ENSP00000399168.2:p.Asp262=
NM_005514.6:c.786T>C	NP_005505.2:p.Asp262=
NM_005514.7:c.786T>C	NP_005505.2:p.Asp262=
ENST00000412585.6:c.786T>C	ENSP00000399168.2:p.Asp262=
ENST00000463574.1:n.377T>C
ENST00000474381.2:n.2833T>C
ENST00000481849.6:n.2259T>C
ENST00000497377.6:n.2259T>C
ENST00000498007.1:n.1052T>C
ENST00000640094.2:c.786T>C	ENSP00000491275.2:p.Asp262=
ENST00000696558.1:c.855T>C	ENSP00000512716.1:n.855T>C
ENST00000696559.1:c.786T>C	ENSP00000512717.1:p.Asp262=
ENST00000696560.1:c.786T>C	ENSP00000512718.1:p.Asp262=
ENST00000696561.1:c.786T>C	ENSP00000512719.1:p.Asp262=
ENST00000696562.1:c.786T>C	ENSP00000512720.1:p.Asp262=
XM_011514556.1:c.819T>C	XP_011512858.1:p.Asp273=
XM_011514557.1:c.786T>C	XP_011512859.1:p.Asp262=
XR_926175.1:n.1225T>C