Canonical Allele Identifier: CA1619077360
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269136A= , CM000668.2:g.31269136A= GRCh38
NC_000006.11:g.31236913A= , CM000668.1:g.31236913A= GRCh37
NC_000006.10:g.31344892A= NCBI36
NG_029422.2:g.7996T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*33T= MANE Select ENSP00000365402.5:n.*33T=
ENST00000376228.9:c.*33T= ENSP00000365402.5:n.*33T=
ENST00000376237.8:c.*721T= ENSP00000365412.4:n.*721T=
ENST00000383329.7:c.*33T= ENSP00000372819.3:n.*33T=
ENST00000466892.5:n.367T=
ENST00000470363.5:n.892T=
ENST00000487245.5:n.1493T=
NM_002117.5:c.*33T= NP_002108.4:n.*33T=
NM_002117.6:c.*33T= MANE Select NP_002108.4:n.*33T=