Canonical Allele Identifier: CA1619077857

Gene: HLA-C

Linked Data

• dbSNP Id: rs1761123755
• gnomAD v4: 6-31269429-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269429G>A , CM000668.2:g.31269429G>A	GRCh38
NC_000006.11:g.31237206G>A , CM000668.1:g.31237206G>A	GRCh37
NC_000006.10:g.31345185G>A	NCBI36
NG_029422.2:g.7703C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1049-44C>T MANE Select	ENSP00000365402.5:n.1049-44C>T
ENST00000376228.9:c.1049-44C>T	ENSP00000365402.5:n.1049-44C>T
ENST00000376237.8:c.*636-44C>T	ENSP00000365412.4:n.*636-44C>T
ENST00000383329.7:c.1067-44C>T	ENSP00000372819.3:n.1067-44C>T
ENST00000466892.5:n.238C>T
ENST00000470363.5:n.807-44C>T
ENST00000487245.5:n.1408-44C>T
NM_002117.5:c.1049-44C>T	NP_002108.4:n.1049-44C>T
NM_002117.6:c.1049-44C>T MANE Select	NP_002108.4:n.1049-44C>T