Canonical Allele Identifier: CA1619114838
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357462_31357464delinsCCT , CM000668.2:g.31357462_31357464delinsCCT GRCh38
NC_000006.11:g.31325239_31325241delinsCCT , CM000668.1:g.31325239_31325241delinsCCT GRCh37
NC_000006.10:g.31433218_31433220delinsCCT NCBI36
NG_023187.1:g.4749_4751delinsAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1338+150_1338+152delinsAGG
ENST00000481849.6:n.1338+150_1338+152delinsAGG
ENST00000497377.6:n.1338+150_1338+152delinsAGG
ENST00000696559.1:c.-136+150_-136+152delinsAGG ENSP00000512717.1:n.-136+150_-136+152delinsAGG
ENST00000696560.1:c.-136+150_-136+152delinsAGG ENSP00000512718.1:n.-136+150_-136+152delinsAGG
ENST00000696561.1:c.-136+150_-136+152delinsAGG ENSP00000512719.1:n.-136+150_-136+152delinsAGG
ENST00000696562.1:c.-135-171_-135-169delinsAGG ENSP00000512720.1:n.-135-171_-135-169delinsAGG
ENST00000603274.1:n.816_818delinsCCT
XR_926692.1:n.164+150_164+152delinsAGG