Canonical Allele Identifier: CA2711119905
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs9279069

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269801_31269802dup , CM000668.2:g.31269801_31269802dup GRCh38
NC_000006.11:g.31237578_31237579dup , CM000668.1:g.31237578_31237579dup GRCh37
NC_000006.10:g.31345557_31345558dup NCBI36
NG_029422.2:g.7332_7333dup

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.1015+166_1015+167dup MANE Select ENSP00000365402.5:n.1015+166_1015+167dup
ENST00000376228.9:c.1015+166_1015+167dup ENSP00000365402.5:n.1015+166_1015+167dup
ENST00000376237.8:c.*602+166_*602+167dup ENSP00000365412.4:n.*602+166_*602+167dup
ENST00000383329.7:c.1015+166_1015+167dup ENSP00000372819.3:n.1015+166_1015+167dup
ENST00000470363.5:n.499_500dup
ENST00000487245.5:n.1374+166_1374+167dup
NM_002117.5:c.1015+166_1015+167dup NP_002108.4:n.1015+166_1015+167dup
NM_002117.6:c.1015+166_1015+167dup MANE Select NP_002108.4:n.1015+166_1015+167dup