Canonical Allele Identifier: CA1619077177
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs9279068

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268942dup , CM000668.2:g.31268942dup GRCh38
NC_000006.11:g.31236719dup , CM000668.1:g.31236719dup GRCh37
NC_000006.10:g.31344698dup NCBI36
NG_029422.2:g.8193dup

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*230dup MANE Select ENSP00000365402.5:n.*230dup
ENST00000376228.9:c.*230dup ENSP00000365402.5:n.*230dup
ENST00000376237.8:c.*918dup ENSP00000365412.4:n.*918dup
ENST00000383329.7:c.*230dup ENSP00000372819.3:n.*230dup
ENST00000466892.5:n.564dup
ENST00000470363.5:n.1089dup
ENST00000487245.5:n.1690dup
NM_002117.5:c.*230dup NP_002108.4:n.*230dup
NM_002117.6:c.*230dup MANE Select NP_002108.4:n.*230dup