Canonical Allele Identifier: CA1619116788
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31359334C= , CM000668.2:g.31359334C= GRCh38
NC_000006.11:g.31327111C= , CM000668.1:g.31327111C= GRCh37
NC_000006.10:g.31435090C= NCBI36
NG_023187.1:g.2879G=

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1271-1653G=
ENST00000481849.6:n.1271-1653G=
ENST00000497377.6:n.1271-1653G=
ENST00000696559.1:c.-203-1653G= ENSP00000512717.1:n.-203-1653G=
ENST00000696560.1:c.-203-1653G= ENSP00000512718.1:n.-203-1653G=
ENST00000696561.1:c.-203-1653G= ENSP00000512719.1:n.-203-1653G=
ENST00000696562.1:c.-135-2041G= ENSP00000512720.1:n.-135-2041G=