Canonical Allele Identifier: CA2677949457

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31269140-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269140T>A , CM000668.2:g.31269140T>A	GRCh38
NC_000006.11:g.31236917T>A , CM000668.1:g.31236917T>A	GRCh37
NC_000006.10:g.31344896T>A	NCBI36
NG_029422.2:g.7992A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.*29A>T MANE Select	ENSP00000365402.5:n.*29A>T
ENST00000376228.9:c.*29A>T	ENSP00000365402.5:n.*29A>T
ENST00000376237.8:c.*717A>T	ENSP00000365412.4:n.*717A>T
ENST00000383329.7:c.*29A>T	ENSP00000372819.3:n.*29A>T
ENST00000466892.5:n.363A>T
ENST00000470363.5:n.888A>T
ENST00000487245.5:n.1489A>T
NM_002117.5:c.*29A>T	NP_002108.4:n.*29A>T
NM_002117.6:c.*29A>T MANE Select	NP_002108.4:n.*29A>T