Canonical Allele Identifier: CA1619114924
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357542_31357543delinsAG , CM000668.2:g.31357542_31357543delinsAG GRCh38
NC_000006.11:g.31325319_31325320delinsAG , CM000668.1:g.31325319_31325320delinsAG GRCh37
NC_000006.10:g.31433298_31433299delinsAG NCBI36
NG_023187.1:g.4670_4671delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1338+71_1338+72delinsCT
ENST00000481849.6:n.1338+71_1338+72delinsCT
ENST00000497377.6:n.1338+71_1338+72delinsCT
ENST00000696559.1:c.-136+71_-136+72delinsCT ENSP00000512717.1:n.-136+71_-136+72delinsCT
ENST00000696560.1:c.-136+71_-136+72delinsCT ENSP00000512718.1:n.-136+71_-136+72delinsCT
ENST00000696561.1:c.-136+71_-136+72delinsCT ENSP00000512719.1:n.-136+71_-136+72delinsCT
ENST00000696562.1:c.-135-250_-135-249delinsCT ENSP00000512720.1:n.-135-250_-135-249delinsCT
ENST00000603274.1:n.896_897delinsAG
XR_926692.1:n.164+71_164+72delinsCT