Canonical Allele Identifier: CA449790452

Gene: HLA-C

Linked Data

• gnomAD v3: 6-31271227-G-A
• gnomAD v4: 6-31271227-G-A
• MyVariant Identifiers: chr6:g.31239004G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271227G>A , CM000668.2:g.31271227G>A	GRCh38
NC_000006.11:g.31239004G>A , CM000668.1:g.31239004G>A	GRCh37
NC_000006.10:g.31346983G>A	NCBI36
NG_029422.2:g.5905C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.465C>T MANE Select	ENSP00000365402.5:p.Arg155=
ENST00000376228.9:c.465C>T	ENSP00000365402.5:p.Arg155=
ENST00000376237.8:c.*52C>T	ENSP00000365412.4:n.*52C>T
ENST00000383329.7:c.465C>T	ENSP00000372819.3:p.Arg155=
ENST00000415537.1:c.463C>T
ENST00000484378.1:n.734C>T
ENST00000487245.5:n.824C>T
ENST00000495835.1:n.654C>T
NM_002117.5:c.465C>T	NP_002108.4:p.Arg155=
NM_002117.6:c.465C>T MANE Select	NP_002108.4:p.Arg155=