Canonical Allele Identifier: CA2320556820

Gene: C3

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_000064.4:c.3281C= MANE Select	NP_000055.2:p.Ala1094=
ENST00000245907.11:c.3281C= MANE Select	ENSP00000245907.4:p.Ala1094=
NM_000064.3:c.3281C=	NP_000055.2:p.Ala1094=
ENST00000245907.10:c.3281C=	ENSP00000245907.4:p.Ala1094=
ENST00000598805.2:n.51C=
ENST00000695651.1:n.1629C=
ENST00000695652.1:c.3158C=	ENSP00000512083.1:p.Ala1053=
ENST00000695653.1:c.1190C=	ENSP00000512084.1:p.Ala397=
ENST00000695654.1:c.2405C=	ENSP00000512085.1:p.Ala802=
ENST00000695655.1:c.2222C=	ENSP00000512086.1:n.2222C=
ENST00000695692.1:n.2645C=