Canonical Allele Identifier: CA403619712

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6686207A>T (hg19) ; chr19:g.6686196A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686196A>T , CM000681.2:g.6686196A>T	GRCh38
NC_000019.9:g.6686207A>T , CM000681.1:g.6686207A>T	GRCh37
NC_000019.8:g.6637207A>T	NCBI36
NG_009557.1:g.39456T>A , LRG_27:g.39456T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2086T>A
ENST00000695652.1:c.3615T>A	ENSP00000512083.1:p.Phe1205Leu
ENST00000695653.1:c.1647T>A	ENSP00000512084.1:p.Phe549Leu
ENST00000695654.1:c.2763T>A	ENSP00000512085.1:p.Phe921Leu
ENST00000695655.1:c.2679T>A	ENSP00000512086.1:n.2679T>A
ENST00000695692.1:n.3102T>A
ENST00000245907.11:c.3738T>A MANE Select	ENSP00000245907.4:p.Phe1246Leu
ENST00000245907.10:c.3738T>A	ENSP00000245907.4:p.Phe1246Leu
ENST00000596238.1:n.181T>A
ENST00000601008.1:c.241+550T>A	ENSP00000471384.1:n.241+550T>A
NM_000064.3:c.3738T>A	NP_000055.2:p.Phe1246Leu
NM_000064.4:c.3738T>A MANE Select	NP_000055.2:p.Phe1246Leu