Canonical Allele Identifier: CA1619118680
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355338T= , CM000668.2:g.31355338T= GRCh38
NC_000006.11:g.31323115T= , CM000668.1:g.31323115T= GRCh37
NC_000006.10:g.31431094T= NCBI36
NG_023187.1:g.6875A=

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.2921A=
ENST00000481849.6:n.2347A=
ENST00000497377.6:n.2347A=
ENST00000640094.2:c.874A= ENSP00000491275.2:p.Lys292=
ENST00000696558.1:c.943A= ENSP00000512716.1:n.943A=
ENST00000696559.1:c.874A= ENSP00000512717.1:p.Lys292=
ENST00000696560.1:c.874A= ENSP00000512718.1:p.Lys292=
ENST00000696561.1:c.874A= ENSP00000512719.1:p.Lys292=
ENST00000696562.1:c.874A= ENSP00000512720.1:p.Lys292=
ENST00000412585.7:c.874A= MANE Select ENSP00000399168.2:p.Lys292=
ENST00000640094.1:c.67A= ENSP00000491275.1:p.Lys23=
ENST00000412585.6:c.874A= ENSP00000399168.2:p.Lys292=
ENST00000463574.1:n.465A=
NM_005514.6:c.874A= NP_005505.2:p.Lys292=
XM_011514556.1:c.907A= XP_011512858.1:p.Lys303=
XM_011514557.1:c.874A= XP_011512859.1:p.Lys292=
XR_926175.1:n.1313A=
NM_005514.7:c.874A= NP_005505.2:p.Lys292=
NM_005514.8:c.874A= MANE Select NP_005505.2:p.Lys292=