Canonical Allele Identifier: CA2677949864

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31269603-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269603G>C , CM000668.2:g.31269603G>C	GRCh38
NC_000006.11:g.31237380G>C , CM000668.1:g.31237380G>C	GRCh37
NC_000006.10:g.31345359G>C	NCBI36
NG_029422.2:g.7529C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1016-78C>G MANE Select	ENSP00000365402.5:n.1016-78C>G
ENST00000376228.9:c.1016-78C>G	ENSP00000365402.5:n.1016-78C>G
ENST00000376237.8:c.*603-78C>G	ENSP00000365412.4:n.*603-78C>G
ENST00000383329.7:c.1016-60C>G	ENSP00000372819.3:n.1016-60C>G
ENST00000466892.5:n.64C>G
ENST00000470363.5:n.696C>G
ENST00000487245.5:n.1375-78C>G
NM_002117.5:c.1016-78C>G	NP_002108.4:n.1016-78C>G
NM_002117.6:c.1016-78C>G MANE Select	NP_002108.4:n.1016-78C>G