Canonical Allele Identifier: CA403612028

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6679154C>T (hg19) ; chr19:g.6679143C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679143C>T , CM000681.2:g.6679143C>T	GRCh38
NC_000019.9:g.6679154C>T , CM000681.1:g.6679154C>T	GRCh37
NC_000019.8:g.6630154C>T	NCBI36
NG_009557.1:g.46509G>A , LRG_27:g.46509G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2960G>A
ENST00000695653.1:c.2521G>A	ENSP00000512084.1:p.Glu841Lys
ENST00000695654.1:c.3637G>A	ENSP00000512085.1:p.Glu1213Lys
ENST00000695689.1:c.583G>A	ENSP00000512101.1:n.583G>A
ENST00000695690.1:n.1677G>A
ENST00000695691.1:n.1473G>A
ENST00000245907.11:c.4612G>A MANE Select	ENSP00000245907.4:p.Glu1538Lys
ENST00000245907.10:c.4612G>A	ENSP00000245907.4:p.Glu1538Lys
ENST00000599668.1:n.232G>A
ENST00000599899.5:n.1571G>A
ENST00000601008.1:c.242-1185G>A	ENSP00000471384.1:n.242-1185G>A
ENST00000602229.1:c.59G>A
NM_000064.3:c.4612G>A	NP_000055.2:p.Glu1538Lys
NM_000064.4:c.4612G>A MANE Select	NP_000055.2:p.Glu1538Lys