Canonical Allele Identifier: CA1619116468
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31354089C= , CM000668.2:g.31354089C= GRCh38
NC_000006.11:g.31321866C= , CM000668.1:g.31321866C= GRCh37
NC_000006.10:g.31429845C= NCBI36
NG_023187.1:g.8124G=

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.3348G=
ENST00000481849.6:n.3308G=
ENST00000497377.6:n.3215G=
ENST00000696558.1:c.1370G= ENSP00000512716.1:n.1370G=
ENST00000696559.1:c.*212G= ENSP00000512717.1:n.*212G=
ENST00000696560.1:c.*212G= ENSP00000512718.1:n.*212G=
ENST00000696561.1:c.*212G= ENSP00000512719.1:n.*212G=
ENST00000696562.1:c.*212G= ENSP00000512720.1:n.*212G=
ENST00000412585.7:c.*212G= MANE Select ENSP00000399168.2:n.*212G=
ENST00000412585.6:c.*212G= ENSP00000399168.2:n.*212G=
ENST00000481849.5:n.536G=
ENST00000497377.5:n.700G=
NM_005514.6:c.*212G= NP_005505.2:n.*212G=
XM_011514556.1:c.*212G= XP_011512858.1:n.*212G=
XM_011514557.1:c.*212G= XP_011512859.1:n.*212G=
XR_926175.1:n.1740G=
NM_005514.7:c.*212G= NP_005505.2:n.*212G=
NM_005514.8:c.*212G= MANE Select NP_005505.2:n.*212G=