Canonical Allele Identifier: CA2677958039
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357315_31357316insTAG , CM000668.2:g.31357315_31357316insTAG GRCh38
NC_000006.11:g.31325092_31325093insTAG , CM000668.1:g.31325092_31325093insTAG GRCh37
NC_000006.10:g.31433071_31433072insTAG NCBI36
NG_023187.1:g.4897_4898insCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1339-23_1339-22insCTA
ENST00000481849.6:n.1339-23_1339-22insCTA
ENST00000497377.6:n.1339-23_1339-22insCTA
ENST00000696559.1:c.-135-23_-135-22insCTA ENSP00000512717.1:n.-135-23_-135-22insCTA
ENST00000696560.1:c.-135-23_-135-22insCTA ENSP00000512718.1:n.-135-23_-135-22insCTA
ENST00000696561.1:c.-135-23_-135-22insCTA ENSP00000512719.1:n.-135-23_-135-22insCTA
ENST00000696562.1:c.-135-23_-135-22insCTA ENSP00000512720.1:n.-135-23_-135-22insCTA
ENST00000603274.1:n.669_670insTAG
XR_926692.1:n.165-23_165-22insCTA