Canonical Allele Identifier: CA1619077218
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269007G= , CM000668.2:g.31269007G= GRCh38
NC_000006.11:g.31236784G= , CM000668.1:g.31236784G= GRCh37
NC_000006.10:g.31344763G= NCBI36
NG_029422.2:g.8125C=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*162C= MANE Select ENSP00000365402.5:n.*162C=
ENST00000376228.9:c.*162C= ENSP00000365402.5:n.*162C=
ENST00000376237.8:c.*850C= ENSP00000365412.4:n.*850C=
ENST00000383329.7:c.*162C= ENSP00000372819.3:n.*162C=
ENST00000466892.5:n.496C=
ENST00000470363.5:n.1021C=
ENST00000487245.5:n.1622C=
NM_002117.5:c.*162C= NP_002108.4:n.*162C=
NM_002117.6:c.*162C= MANE Select NP_002108.4:n.*162C=