Canonical Allele Identifier: CA2813436488

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686329C>A , CM000681.2:g.6686329C>A	GRCh38
NC_000019.9:g.6686340C>A , CM000681.1:g.6686340C>A	GRCh37
NC_000019.8:g.6637340C>A	NCBI36
NG_009557.1:g.39323G>T , LRG_27:g.39323G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1995-42G>T
ENST00000695652.1:c.3524-42G>T	ENSP00000512083.1:n.3524-42G>T
ENST00000695653.1:c.1556-42G>T	ENSP00000512084.1:n.1556-42G>T
ENST00000695654.1:c.2672-42G>T	ENSP00000512085.1:n.2672-42G>T
ENST00000695655.1:c.2588-42G>T	ENSP00000512086.1:n.2588-42G>T
ENST00000695692.1:n.3011-42G>T
ENST00000245907.11:c.3647-42G>T MANE Select	ENSP00000245907.4:n.3647-42G>T
ENST00000245907.10:c.3647-42G>T	ENSP00000245907.4:n.3647-42G>T
ENST00000596238.1:n.48G>T
ENST00000598805.2:n.833G>T
ENST00000601008.1:c.241+417G>T	ENSP00000471384.1:n.241+417G>T
NM_000064.3:c.3647-42G>T	NP_000055.2:n.3647-42G>T
NM_000064.4:c.3647-42G>T MANE Select	NP_000055.2:n.3647-42G>T