Canonical Allele Identifier: CA403639559

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6709825T>C (hg19) ; chr19:g.6709814T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709814T>C , CM000681.2:g.6709814T>C	GRCh38
NC_000019.9:g.6709825T>C , CM000681.1:g.6709825T>C	GRCh37
NC_000019.8:g.6660825T>C	NCBI36
NG_009557.1:g.15838A>G , LRG_27:g.15838A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1592A>G	ENSP00000512083.1:p.Asp531Gly
ENST00000695654.1:c.839A>G	ENSP00000512085.1:p.Asp280Gly
ENST00000695655.1:c.656A>G	ENSP00000512086.1:n.656A>G
ENST00000695692.1:n.1079A>G
ENST00000245907.11:c.1715A>G MANE Select	ENSP00000245907.4:p.Asp572Gly
ENST00000245907.10:c.1715A>G	ENSP00000245907.4:p.Asp572Gly
ENST00000600763.1:n.348A>G
NM_000064.3:c.1715A>G	NP_000055.2:p.Asp572Gly
NM_000064.4:c.1715A>G MANE Select	NP_000055.2:p.Asp572Gly