Canonical Allele Identifier: CA9129168

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6707114C>T , CM000681.2:g.6707114C>T	GRCh38
NC_000019.9:g.6707125C>T , CM000681.1:g.6707125C>T	GRCh37
NC_000019.8:g.6658125C>T	NCBI36
NG_009557.1:g.18538G>A , LRG_27:g.18538G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000064.4:c.2207G>A MANE Select	NP_000055.2:p.Arg736Gln
ENST00000245907.11:c.2207G>A MANE Select	ENSP00000245907.4:p.Arg736Gln
NM_000064.3:c.2207G>A	NP_000055.2:p.Arg736Gln
ENST00000245907.10:c.2207G>A	ENSP00000245907.4:p.Arg736Gln
ENST00000695651.1:n.478G>A
ENST00000695652.1:c.2084G>A	ENSP00000512083.1:p.Arg695Gln
ENST00000695653.1:c.116G>A	ENSP00000512084.1:p.Arg39Gln
ENST00000695654.1:c.1331G>A	ENSP00000512085.1:p.Arg444Gln
ENST00000695655.1:c.1148G>A	ENSP00000512086.1:n.1148G>A
ENST00000695692.1:n.1571G>A