Canonical Allele Identifier: CA2677957933
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357178_31357179del , CM000668.2:g.31357178_31357179del GRCh38
NC_000006.11:g.31324955_31324956del , CM000668.1:g.31324955_31324956del GRCh37
NC_000006.10:g.31432934_31432935del NCBI36
NG_023187.1:g.5036_5037del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1455_1456del
ENST00000481849.6:n.1455_1456del
ENST00000497377.6:n.1455_1456del
ENST00000696559.1:c.-19_-18del ENSP00000512717.1:n.-19_-18del
ENST00000696560.1:c.-19_-18del ENSP00000512718.1:n.-19_-18del
ENST00000696561.1:c.-19_-18del ENSP00000512719.1:n.-19_-18del
ENST00000696562.1:c.-19_-18del ENSP00000512720.1:n.-19_-18del
ENST00000412585.7:c.-19_-18del MANE Select ENSP00000399168.2:n.-19_-18del
ENST00000412585.6:c.-19_-18del ENSP00000399168.2:n.-19_-18del
ENST00000434333.1:c.-114_-113del ENSP00000405931.1:n.-114_-113del
ENST00000498007.1:n.3_4del
ENST00000603274.1:n.532_533del
NM_005514.6:c.-19_-18del NP_005505.2:n.-19_-18del
NM_005514.7:c.-19_-18del NP_005505.2:n.-19_-18del
NM_005514.8:c.-19_-18del MANE Select NP_005505.2:n.-19_-18del