Canonical Allele Identifier: CA136836759
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs796100503

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357246_31357253delinsCACCCGAC , CM000668.2:g.31357246_31357253delinsCACCCGAC GRCh38
NC_000006.11:g.31325023_31325030delinsCACCCGAC , CM000668.1:g.31325023_31325030delinsCACCCGAC GRCh37
NC_000006.10:g.31433002_31433009delinsCACCCGAC NCBI36
NG_023187.1:g.4960_4967delinsGTCGGGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1379_1386delinsGTCGGGTG
ENST00000481849.6:n.1379_1386delinsGTCGGGTG
ENST00000497377.6:n.1379_1386delinsGTCGGGTG
ENST00000696559.1:c.-95_-88delinsGTCGGGTG ENSP00000512717.1:n.-95_-88delinsGTCGGGTG
ENST00000696560.1:c.-95_-88delinsGTCGGGTG ENSP00000512718.1:n.-95_-88delinsGTCGGGTG
ENST00000696561.1:c.-95_-88delinsGTCGGGTG ENSP00000512719.1:n.-95_-88delinsGTCGGGTG
ENST00000696562.1:c.-95_-88delinsGTCGGGTG ENSP00000512720.1:n.-95_-88delinsGTCGGGTG
ENST00000603274.1:n.600_607delinsCACCCGAC