Canonical Allele Identifier: CA136868719

Gene: HLA-C

Linked Data

• dbSNP Id: rs11547351
• gnomAD v4: 6-31271646-C-G
• MyVariant Identifiers: chr6:g.31239423C>G (hg19) ; chr6:g.31271646C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271646C>G , CM000668.2:g.31271646C>G	GRCh38
NC_000006.11:g.31239423C>G , CM000668.1:g.31239423C>G	GRCh37
NC_000006.10:g.31347402C>G	NCBI36
NG_029422.2:g.5486G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.296G>C MANE Select	ENSP00000365402.5:p.Arg99Pro
ENST00000376228.9:c.296G>C	ENSP00000365402.5:p.Arg99Pro
ENST00000376237.8:c.296G>C	ENSP00000365412.4:p.Arg99Pro
ENST00000383329.7:c.296G>C	ENSP00000372819.3:p.Arg99Pro
ENST00000415537.1:c.294G>C
ENST00000484378.1:n.315G>C
ENST00000487245.5:n.405G>C
ENST00000495835.1:n.485G>C
NM_002117.5:c.296G>C	NP_002108.4:p.Arg99Pro
NM_002117.6:c.296G>C MANE Select	NP_002108.4:p.Arg99Pro