Canonical Allele Identifier: CA403634055

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697763T>C (hg19) ; chr19:g.6697752T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697752T>C , CM000681.2:g.6697752T>C	GRCh38
NC_000019.9:g.6697763T>C , CM000681.1:g.6697763T>C	GRCh37
NC_000019.8:g.6648763T>C	NCBI36
NG_009557.1:g.27900A>G , LRG_27:g.27900A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.831A>G
ENST00000695652.1:c.2360A>G	ENSP00000512083.1:p.Asp787Gly
ENST00000695653.1:c.392A>G	ENSP00000512084.1:p.Asp131Gly
ENST00000695654.1:c.1607A>G	ENSP00000512085.1:p.Asp536Gly
ENST00000695655.1:c.1424A>G	ENSP00000512086.1:n.1424A>G
ENST00000695692.1:n.1847A>G
ENST00000245907.11:c.2483A>G MANE Select	ENSP00000245907.4:p.Asp828Gly
ENST00000245907.10:c.2483A>G	ENSP00000245907.4:p.Asp828Gly
ENST00000602053.1:n.531A>G
NM_000064.3:c.2483A>G	NP_000055.2:p.Asp828Gly
NM_000064.4:c.2483A>G MANE Select	NP_000055.2:p.Asp828Gly