Canonical Allele Identifier: CA403619406

Gene: C3

Linked Data

• COSMIC: COSM1711659
• MyVariant Identifiers: chr19:g.6686154C>T (hg19) ; chr19:g.6686143C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686143C>T , CM000681.2:g.6686143C>T	GRCh38
NC_000019.9:g.6686154C>T , CM000681.1:g.6686154C>T	GRCh37
NC_000019.8:g.6637154C>T	NCBI36
NG_009557.1:g.39509G>A , LRG_27:g.39509G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2139G>A
ENST00000695652.1:c.3668G>A	ENSP00000512083.1:p.Gly1223Asp
ENST00000695653.1:c.1700G>A	ENSP00000512084.1:p.Gly567Asp
ENST00000695654.1:c.2816G>A	ENSP00000512085.1:p.Gly939Asp
ENST00000695655.1:c.2732G>A	ENSP00000512086.1:n.2732G>A
ENST00000695692.1:n.3155G>A
ENST00000245907.11:c.3791G>A MANE Select	ENSP00000245907.4:p.Gly1264Asp
ENST00000245907.10:c.3791G>A	ENSP00000245907.4:p.Gly1264Asp
ENST00000596238.1:n.234G>A
ENST00000601008.1:c.241+603G>A	ENSP00000471384.1:n.241+603G>A
NM_000064.3:c.3791G>A	NP_000055.2:p.Gly1264Asp
NM_000064.4:c.3791G>A MANE Select	NP_000055.2:p.Gly1264Asp