Canonical Allele Identifier: CA403626315

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6693033G>T , CM000681.2:g.6693033G>T	GRCh38
NC_000019.9:g.6693044G>T , CM000681.1:g.6693044G>T	GRCh37
NC_000019.8:g.6644044G>T	NCBI36
NG_009557.1:g.32619C>A , LRG_27:g.32619C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000064.4:c.3281C>A MANE Select	NP_000055.2:p.Ala1094Asp
ENST00000245907.11:c.3281C>A MANE Select	ENSP00000245907.4:p.Ala1094Asp
NM_000064.3:c.3281C>A	NP_000055.2:p.Ala1094Asp
ENST00000245907.10:c.3281C>A	ENSP00000245907.4:p.Ala1094Asp
ENST00000598805.2:n.51C>A
ENST00000695651.1:n.1629C>A
ENST00000695652.1:c.3158C>A	ENSP00000512083.1:p.Ala1053Asp
ENST00000695653.1:c.1190C>A	ENSP00000512084.1:p.Ala397Asp
ENST00000695654.1:c.2405C>A	ENSP00000512085.1:p.Ala802Asp
ENST00000695655.1:c.2222C>A	ENSP00000512086.1:n.2222C>A
ENST00000695692.1:n.2645C>A