Canonical Allele Identifier: CA9128868

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6694561C>T , CM000681.2:g.6694561C>T	GRCh38
NC_000019.9:g.6694572C>T , CM000681.1:g.6694572C>T	GRCh37
NC_000019.8:g.6645572C>T	NCBI36
NG_009557.1:g.31091G>A , LRG_27:g.31091G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000064.4:c.3024G>A MANE Select	NP_000055.2:p.Ser1008=
ENST00000245907.11:c.3024G>A MANE Select	ENSP00000245907.4:p.Ser1008=
NM_000064.3:c.3024G>A	NP_000055.2:p.Ser1008=
ENST00000245907.10:c.3024G>A	ENSP00000245907.4:p.Ser1008=
ENST00000695651.1:n.1372G>A
ENST00000695652.1:c.2901G>A	ENSP00000512083.1:p.Ser967=
ENST00000695653.1:c.933G>A	ENSP00000512084.1:p.Ser311=
ENST00000695654.1:c.2148G>A	ENSP00000512085.1:p.Ser716=
ENST00000695655.1:c.1965G>A	ENSP00000512086.1:n.1965G>A
ENST00000695692.1:n.2388G>A