Canonical Allele Identifier: CA2677949032

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31268861-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31268861G>A , CM000668.2:g.31268861G>A	GRCh38
NC_000006.11:g.31236638G>A , CM000668.1:g.31236638G>A	GRCh37
NC_000006.10:g.31344617G>A	NCBI36
NG_029422.2:g.8271C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.*308C>T MANE Select	ENSP00000365402.5:n.*308C>T
ENST00000376228.9:c.*308C>T	ENSP00000365402.5:n.*308C>T
ENST00000376237.8:c.*996C>T	ENSP00000365412.4:n.*996C>T
ENST00000383329.7:c.*308C>T	ENSP00000372819.3:n.*308C>T
ENST00000466892.5:n.642C>T
ENST00000470363.5:n.1167C>T
ENST00000487245.5:n.1768C>T
NM_002117.5:c.*308C>T	NP_002108.4:n.*308C>T
NM_002117.6:c.*308C>T MANE Select	NP_002108.4:n.*308C>T