Canonical Allele Identifier: CA2677949467

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31269155-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269155C>A , CM000668.2:g.31269155C>A	GRCh38
NC_000006.11:g.31236932C>A , CM000668.1:g.31236932C>A	GRCh37
NC_000006.10:g.31344911C>A	NCBI36
NG_029422.2:g.7977G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.*14G>T MANE Select	ENSP00000365402.5:n.*14G>T
ENST00000376228.9:c.*14G>T	ENSP00000365402.5:n.*14G>T
ENST00000376237.8:c.*702G>T	ENSP00000365412.4:n.*702G>T
ENST00000383329.7:c.*14G>T	ENSP00000372819.3:n.*14G>T
ENST00000466892.5:n.348G>T
ENST00000470363.5:n.873G>T
ENST00000487245.5:n.1474G>T
NM_002117.5:c.*14G>T	NP_002108.4:n.*14G>T
NM_002117.6:c.*14G>T MANE Select	NP_002108.4:n.*14G>T