Canonical Allele Identifier: CA2711121898
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs67384697

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268907dup , CM000668.2:g.31268907dup GRCh38
NC_000006.11:g.31236684dup , CM000668.1:g.31236684dup GRCh37
NC_000006.10:g.31344663dup NCBI36
NG_029422.2:g.8226dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*263dup MANE Select ENSP00000365402.5:n.*263dup
ENST00000376228.9:c.*263dup ENSP00000365402.5:n.*263dup
ENST00000376237.8:c.*951dup ENSP00000365412.4:n.*951dup
ENST00000383329.7:c.*263dup ENSP00000372819.3:n.*263dup
ENST00000466892.5:n.597dup
ENST00000470363.5:n.1122dup
ENST00000487245.5:n.1723dup
NM_002117.5:c.*263dup NP_002108.4:n.*263dup
NM_002117.6:c.*263dup MANE Select NP_002108.4:n.*263dup