Canonical Allele Identifier: CA136836716
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs45496696

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356958del , CM000668.2:g.31356958del GRCh38
NC_000006.11:g.31324735del , CM000668.1:g.31324735del GRCh37
NC_000006.10:g.31432714del NCBI36
NG_023187.1:g.5256del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1547del
ENST00000481849.6:n.1547del
ENST00000497377.6:n.1547del
ENST00000640094.2:c.74del
ENST00000696558.1:c.74del
ENST00000696559.1:c.74del
ENST00000696560.1:c.74del
ENST00000696561.1:c.74del
ENST00000696562.1:c.74del
ENST00000412585.7:c.74del
ENST00000412585.6:c.74del
ENST00000434333.1:c.107del ENSP00000405931.1:p.Gly36AlafsTer5
ENST00000498007.1:n.95del
ENST00000603274.1:n.312del
NM_005514.6:c.74del
XM_011514556.1:c.107del XP_011512858.1:p.Gly36AlafsTer5
XM_011514557.1:c.74del
XR_926175.1:n.84del
NM_005514.7:c.74del
NM_005514.8:c.74del