Canonical Allele Identifier: CA403619715

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6686208A>T (hg19) ; chr19:g.6686197A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686197A>T , CM000681.2:g.6686197A>T	GRCh38
NC_000019.9:g.6686208A>T , CM000681.1:g.6686208A>T	GRCh37
NC_000019.8:g.6637208A>T	NCBI36
NG_009557.1:g.39455T>A , LRG_27:g.39455T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2085T>A
ENST00000695652.1:c.3614T>A	ENSP00000512083.1:p.Phe1205Tyr
ENST00000695653.1:c.1646T>A	ENSP00000512084.1:p.Phe549Tyr
ENST00000695654.1:c.2762T>A	ENSP00000512085.1:p.Phe921Tyr
ENST00000695655.1:c.2678T>A	ENSP00000512086.1:n.2678T>A
ENST00000695692.1:n.3101T>A
ENST00000245907.11:c.3737T>A MANE Select	ENSP00000245907.4:p.Phe1246Tyr
ENST00000245907.10:c.3737T>A	ENSP00000245907.4:p.Phe1246Tyr
ENST00000596238.1:n.180T>A
ENST00000601008.1:c.241+549T>A	ENSP00000471384.1:n.241+549T>A
NM_000064.3:c.3737T>A	NP_000055.2:p.Phe1246Tyr
NM_000064.4:c.3737T>A MANE Select	NP_000055.2:p.Phe1246Tyr