Canonical Allele Identifier: CA2677958023
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357247_31357248insCCCG , CM000668.2:g.31357247_31357248insCCCG GRCh38
NC_000006.11:g.31325024_31325025insCCCG , CM000668.1:g.31325024_31325025insCCCG GRCh37
NC_000006.10:g.31433003_31433004insCCCG NCBI36
NG_023187.1:g.4965_4966insCGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1384_1385insCGGG
ENST00000481849.6:n.1384_1385insCGGG
ENST00000497377.6:n.1384_1385insCGGG
ENST00000696559.1:c.-90_-89insCGGG ENSP00000512717.1:n.-90_-89insCGGG
ENST00000696560.1:c.-90_-89insCGGG ENSP00000512718.1:n.-90_-89insCGGG
ENST00000696561.1:c.-90_-89insCGGG ENSP00000512719.1:n.-90_-89insCGGG
ENST00000696562.1:c.-90_-89insCGGG ENSP00000512720.1:n.-90_-89insCGGG
ENST00000603274.1:n.601_602insCCCG