Canonical Allele Identifier: CA1619114976
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357608_31357612delinsCCTTA , CM000668.2:g.31357608_31357612delinsCCTTA GRCh38
NC_000006.11:g.31325385_31325389delinsCCTTA , CM000668.1:g.31325385_31325389delinsCCTTA GRCh37
NC_000006.10:g.31433364_31433368delinsCCTTA NCBI36
NG_023187.1:g.4601_4605delinsTAAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1338+2_1338+6delinsTAAGG
ENST00000481849.6:n.1338+2_1338+6delinsTAAGG
ENST00000497377.6:n.1338+2_1338+6delinsTAAGG
ENST00000696559.1:c.-136+2_-136+6delinsTAAGG ENSP00000512717.1:n.-136+2_-136+6delinsTAAGG
ENST00000696560.1:c.-136+2_-136+6delinsTAAGG ENSP00000512718.1:n.-136+2_-136+6delinsTAAGG
ENST00000696561.1:c.-136+2_-136+6delinsTAAGG ENSP00000512719.1:n.-136+2_-136+6delinsTAAGG
ENST00000696562.1:c.-135-319_-135-315delinsTAAGG ENSP00000512720.1:n.-135-319_-135-315delinsTAAGG
ENST00000603274.1:n.962_966delinsCCTTA
XR_926692.1:n.164+2_164+6delinsTAAGG