Canonical Allele Identifier: CA449790355

Gene: HLA-C

Linked Data

• gnomAD v3: 6-31271167-A-T
• gnomAD v4: 6-31271167-A-T
• MyVariant Identifiers: chr6:g.31238944A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271167A>T , CM000668.2:g.31271167A>T	GRCh38
NC_000006.11:g.31238944A>T , CM000668.1:g.31238944A>T	GRCh37
NC_000006.10:g.31346923A>T	NCBI36
NG_029422.2:g.5965T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.525T>A MANE Select	ENSP00000365402.5:p.Arg175=
ENST00000376228.9:c.525T>A	ENSP00000365402.5:p.Arg175=
ENST00000376237.8:c.*112T>A	ENSP00000365412.4:n.*112T>A
ENST00000383329.7:c.525T>A	ENSP00000372819.3:p.Arg175=
ENST00000415537.1:c.523T>A
ENST00000484378.1:n.794T>A
ENST00000487245.5:n.884T>A
ENST00000495835.1:n.714T>A
NM_002117.5:c.525T>A	NP_002108.4:p.Arg175=
NM_002117.6:c.525T>A MANE Select	NP_002108.4:p.Arg175=