Canonical Allele Identifier: CA363325805

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31271205-C-T
• MyVariant Identifiers: chr6:g.31238982C>T (hg19) ; chr6:g.31271205C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271205C>T , CM000668.2:g.31271205C>T	GRCh38
NC_000006.11:g.31238982C>T , CM000668.1:g.31238982C>T	GRCh37
NC_000006.10:g.31346961C>T	NCBI36
NG_029422.2:g.5927G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.487G>A MANE Select	ENSP00000365402.5:p.Ala163Thr
ENST00000376228.9:c.487G>A	ENSP00000365402.5:p.Ala163Thr
ENST00000376237.8:c.*74G>A	ENSP00000365412.4:n.*74G>A
ENST00000383329.7:c.487G>A	ENSP00000372819.3:p.Ala163Thr
ENST00000415537.1:c.485G>A
ENST00000484378.1:n.756G>A
ENST00000487245.5:n.846G>A
ENST00000495835.1:n.676G>A
NM_002117.5:c.487G>A	NP_002108.4:p.Ala163Thr
NM_002117.6:c.487G>A MANE Select	NP_002108.4:p.Ala163Thr