Canonical Allele Identifier: CA1619114833
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357460_31357461delinsAG , CM000668.2:g.31357460_31357461delinsAG GRCh38
NC_000006.11:g.31325237_31325238delinsAG , CM000668.1:g.31325237_31325238delinsAG GRCh37
NC_000006.10:g.31433216_31433217delinsAG NCBI36
NG_023187.1:g.4752_4753delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1338+153_1338+154delinsCT
ENST00000481849.6:n.1338+153_1338+154delinsCT
ENST00000497377.6:n.1338+153_1338+154delinsCT
ENST00000696559.1:c.-136+153_-136+154delinsCT ENSP00000512717.1:n.-136+153_-136+154delinsCT
ENST00000696560.1:c.-136+153_-136+154delinsCT ENSP00000512718.1:n.-136+153_-136+154delinsCT
ENST00000696561.1:c.-136+153_-136+154delinsCT ENSP00000512719.1:n.-136+153_-136+154delinsCT
ENST00000696562.1:c.-135-168_-135-167delinsCT ENSP00000512720.1:n.-135-168_-135-167delinsCT
ENST00000603274.1:n.814_815delinsAG
XR_926692.1:n.164+153_164+154delinsCT