Canonical Allele Identifier: CA1619116307
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31353913C= , CM000668.2:g.31353913C= GRCh38
NC_000006.11:g.31321690C= , CM000668.1:g.31321690C= GRCh37
NC_000006.10:g.31429669C= NCBI36
NG_023187.1:g.8300G=

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.3524G=
ENST00000481849.6:n.3484G=
ENST00000497377.6:n.3391G=
ENST00000696558.1:c.1546G= ENSP00000512716.1:n.1546G=
ENST00000696559.1:c.*388G= ENSP00000512717.1:n.*388G=
ENST00000696560.1:c.*388G= ENSP00000512718.1:n.*388G=
ENST00000696561.1:c.*388G= ENSP00000512719.1:n.*388G=
ENST00000696562.1:c.*388G= ENSP00000512720.1:n.*388G=
ENST00000412585.7:c.*388G= MANE Select ENSP00000399168.2:n.*388G=
ENST00000412585.6:c.*388G= ENSP00000399168.2:n.*388G=
ENST00000481849.5:n.712G=
ENST00000497377.5:n.876G=
NM_005514.6:c.*388G= NP_005505.2:n.*388G=
XM_011514556.1:c.*388G= XP_011512858.1:n.*388G=
XM_011514557.1:c.*388G= XP_011512859.1:n.*388G=
XR_926175.1:n.1916G=
NM_005514.7:c.*388G= NP_005505.2:n.*388G=
NM_005514.8:c.*388G= MANE Select NP_005505.2:n.*388G=