Canonical Allele Identifier: CA823883896
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs1457368389

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31359236del , CM000668.2:g.31359236del GRCh38
NC_000006.11:g.31327013del , CM000668.1:g.31327013del GRCh37
NC_000006.10:g.31434992del NCBI36
NG_023187.1:g.2979del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1271-1553del
ENST00000481849.6:n.1271-1553del
ENST00000497377.6:n.1271-1553del
ENST00000696559.1:c.-203-1553del ENSP00000512717.1:n.-203-1553del
ENST00000696560.1:c.-203-1553del ENSP00000512718.1:n.-203-1553del
ENST00000696561.1:c.-203-1553del ENSP00000512719.1:n.-203-1553del
ENST00000696562.1:c.-135-1941del ENSP00000512720.1:n.-135-1941del