Canonical Allele Identifier: CA2320550285

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679181T= , CM000681.2:g.6679181T=	GRCh38
NC_000019.9:g.6679192T= , CM000681.1:g.6679192T=	GRCh37
NC_000019.8:g.6630192T=	NCBI36
NG_009557.1:g.46471A= , LRG_27:g.46471A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2922A=
ENST00000695653.1:c.2483A=	ENSP00000512084.1:p.Asp828=
ENST00000695654.1:c.3599A=	ENSP00000512085.1:p.Asp1200=
ENST00000695689.1:c.545A=	ENSP00000512101.1:n.545A=
ENST00000695690.1:n.1639A=
ENST00000695691.1:n.1435A=
ENST00000245907.11:c.4574A= MANE Select	ENSP00000245907.4:p.Asp1525=
ENST00000245907.10:c.4574A=	ENSP00000245907.4:p.Asp1525=
ENST00000599668.1:n.194A=
ENST00000599899.5:n.1533A=
ENST00000601008.1:c.242-1223A=	ENSP00000471384.1:n.242-1223A=
ENST00000602229.1:c.21A=
NM_000064.3:c.4574A=	NP_000055.2:p.Asp1525=
NM_000064.4:c.4574A= MANE Select	NP_000055.2:p.Asp1525=