Canonical Allele Identifier: CA136866932

Gene: HLA-C

Linked Data

• dbSNP Id: rs281860504
• gnomAD v4: 6-31271185-G-C
• MyVariant Identifiers: chr6:g.31238962G>C (hg19) ; chr6:g.31271185G>C (hg38)

Genomic Alleles

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

Transcript Alleles

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