Canonical Allele Identifier: CA2677949029

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31268855-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31268855T>A , CM000668.2:g.31268855T>A	GRCh38
NC_000006.11:g.31236632T>A , CM000668.1:g.31236632T>A	GRCh37
NC_000006.10:g.31344611T>A	NCBI36
NG_029422.2:g.8277A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.*314A>T MANE Select	ENSP00000365402.5:n.*314A>T
ENST00000376228.9:c.*314A>T	ENSP00000365402.5:n.*314A>T
ENST00000376237.8:c.*1002A>T	ENSP00000365412.4:n.*1002A>T
ENST00000383329.7:c.*314A>T	ENSP00000372819.3:n.*314A>T
ENST00000466892.5:n.648A>T
ENST00000470363.5:n.1173A>T
ENST00000487245.5:n.1774A>T
NM_002117.5:c.*314A>T	NP_002108.4:n.*314A>T
NM_002117.6:c.*314A>T MANE Select	NP_002108.4:n.*314A>T