Canonical Allele Identifier: CA2677949366
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269083T>A , CM000668.2:g.31269083T>A GRCh38
NC_000006.11:g.31236860T>A , CM000668.1:g.31236860T>A GRCh37
NC_000006.10:g.31344839T>A NCBI36
NG_029422.2:g.8049A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*86A>T MANE Select ENSP00000365402.5:n.*86A>T
ENST00000376228.9:c.*86A>T ENSP00000365402.5:n.*86A>T
ENST00000376237.8:c.*774A>T ENSP00000365412.4:n.*774A>T
ENST00000383329.7:c.*86A>T ENSP00000372819.3:n.*86A>T
ENST00000466892.5:n.420A>T
ENST00000470363.5:n.945A>T
ENST00000487245.5:n.1546A>T
NM_002117.5:c.*86A>T NP_002108.4:n.*86A>T
NM_002117.6:c.*86A>T MANE Select NP_002108.4:n.*86A>T