Canonical Allele Identifier: CA449790380
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v3: 6-31271185-G-A
gnomAD v4: 6-31271185-G-A
MyVariant Identifiers: chr6:g.31238962G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271185G>A , CM000668.2:g.31271185G>A GRCh38
NC_000006.11:g.31238962G>A , CM000668.1:g.31238962G>A GRCh37
NC_000006.10:g.31346941G>A NCBI36
NG_029422.2:g.5947C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.507C>T MANE Select ENSP00000365402.5:p.Arg169=
ENST00000376228.9:c.507C>T ENSP00000365402.5:p.Arg169=
ENST00000376237.8:c.*94C>T ENSP00000365412.4:n.*94C>T
ENST00000383329.7:c.507C>T ENSP00000372819.3:p.Arg169=
ENST00000415537.1:c.505C>T
ENST00000484378.1:n.776C>T
ENST00000487245.5:n.866C>T
ENST00000495835.1:n.696C>T
NM_002117.5:c.507C>T NP_002108.4:p.Arg169=
NM_002117.6:c.507C>T MANE Select NP_002108.4:p.Arg169=