Canonical Allele Identifier: CA449790366

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31271176-C-T
• MyVariant Identifiers: chr6:g.31238953C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271176C>T , CM000668.2:g.31271176C>T	GRCh38
NC_000006.11:g.31238953C>T , CM000668.1:g.31238953C>T	GRCh37
NC_000006.10:g.31346932C>T	NCBI36
NG_029422.2:g.5956G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.516G>A MANE Select	ENSP00000365402.5:p.Glu172=
ENST00000376228.9:c.516G>A	ENSP00000365402.5:p.Glu172=
ENST00000376237.8:c.*103G>A	ENSP00000365412.4:n.*103G>A
ENST00000383329.7:c.516G>A	ENSP00000372819.3:p.Glu172=
ENST00000415537.1:c.514G>A
ENST00000484378.1:n.785G>A
ENST00000487245.5:n.875G>A
ENST00000495835.1:n.705G>A
NM_002117.5:c.516G>A	NP_002108.4:p.Glu172=
NM_002117.6:c.516G>A MANE Select	NP_002108.4:p.Glu172=