Canonical Allele Identifier: CA1619077367
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269142C= , CM000668.2:g.31269142C= GRCh38
NC_000006.11:g.31236919C= , CM000668.1:g.31236919C= GRCh37
NC_000006.10:g.31344898C= NCBI36
NG_029422.2:g.7990G=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*27G= MANE Select ENSP00000365402.5:n.*27G=
ENST00000376228.9:c.*27G= ENSP00000365402.5:n.*27G=
ENST00000376237.8:c.*715G= ENSP00000365412.4:n.*715G=
ENST00000383329.7:c.*27G= ENSP00000372819.3:n.*27G=
ENST00000466892.5:n.361G=
ENST00000470363.5:n.886G=
ENST00000487245.5:n.1487G=
NM_002117.5:c.*27G= NP_002108.4:n.*27G=
NM_002117.6:c.*27G= MANE Select NP_002108.4:n.*27G=