Canonical Allele Identifier: CA1619080077
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270668T= , CM000668.2:g.31270668T= GRCh38
NC_000006.11:g.31238445T= , CM000668.1:g.31238445T= GRCh37
NC_000006.10:g.31346424T= NCBI36
NG_029422.2:g.6464A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.620-183A= MANE Select ENSP00000365402.5:n.620-183A=
ENST00000376228.9:c.620-183A= ENSP00000365402.5:n.620-183A=
ENST00000376237.8:c.*207-183A= ENSP00000365412.4:n.*207-183A=
ENST00000383329.7:c.620-183A= ENSP00000372819.3:n.620-183A=
ENST00000415537.1:c.618-183A=
ENST00000487245.5:n.979-183A=
ENST00000495835.1:n.809-183A=
NM_002117.5:c.620-183A= NP_002108.4:n.620-183A=
NM_002117.6:c.620-183A= MANE Select NP_002108.4:n.620-183A=