Canonical Allele Identifier: CA403639497

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6709804T>C (hg19) ; chr19:g.6709793T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709793T>C , CM000681.2:g.6709793T>C	GRCh38
NC_000019.9:g.6709804T>C , CM000681.1:g.6709804T>C	GRCh37
NC_000019.8:g.6660804T>C	NCBI36
NG_009557.1:g.15859A>G , LRG_27:g.15859A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1613A>G	ENSP00000512083.1:p.Gln538Arg
ENST00000695654.1:c.860A>G	ENSP00000512085.1:p.Gln287Arg
ENST00000695655.1:c.677A>G	ENSP00000512086.1:n.677A>G
ENST00000695692.1:n.1100A>G
ENST00000245907.11:c.1736A>G MANE Select	ENSP00000245907.4:p.Gln579Arg
ENST00000245907.10:c.1736A>G	ENSP00000245907.4:p.Gln579Arg
ENST00000600763.1:n.369A>G
NM_000064.3:c.1736A>G	NP_000055.2:p.Gln579Arg
NM_000064.4:c.1736A>G MANE Select	NP_000055.2:p.Gln579Arg