Canonical Allele Identifier: CA449609787

Gene: HLA-C

Linked Data

• gnomAD v3: 6-31269521-T-A
• gnomAD v4: 6-31269521-T-A
• MyVariant Identifiers: chr6:g.31237298T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269521T>A , CM000668.2:g.31269521T>A	GRCh38
NC_000006.11:g.31237298T>A , CM000668.1:g.31237298T>A	GRCh37
NC_000006.10:g.31345277T>A	NCBI36
NG_029422.2:g.7611A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1020A>T MANE Select	ENSP00000365402.5:p.Gly340=
ENST00000376228.9:c.1020A>T	ENSP00000365402.5:p.Gly340=
ENST00000376237.8:c.*607A>T	ENSP00000365412.4:n.*607A>T
ENST00000383329.7:c.1038A>T	ENSP00000372819.3:p.Gly346=
ENST00000466892.5:n.146A>T
ENST00000470363.5:n.778A>T
ENST00000487245.5:n.1379A>T
NM_002117.5:c.1020A>T	NP_002108.4:p.Gly340=
NM_002117.6:c.1020A>T MANE Select	NP_002108.4:p.Gly340=