Canonical Allele Identifier: CA2320550213

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679007A= , CM000681.2:g.6679007A=	GRCh38
NC_000019.9:g.6679018A= , CM000681.1:g.6679018A=	GRCh37
NC_000019.8:g.6630018A=	NCBI36
NG_009557.1:g.46645T= , LRG_27:g.46645T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2978+118T=
ENST00000695653.1:c.2539+118T=	ENSP00000512084.1:n.2539+118T=
ENST00000695654.1:c.3655+118T=	ENSP00000512085.1:n.3655+118T=
ENST00000695689.1:c.601+118T=	ENSP00000512101.1:n.601+118T=
ENST00000695690.1:n.1695+118T=
ENST00000695691.1:n.1491+118T=
ENST00000245907.11:c.4630+118T= MANE Select	ENSP00000245907.4:n.4630+118T=
ENST00000245907.10:c.4630+118T=	ENSP00000245907.4:n.4630+118T=
ENST00000599668.1:n.250+118T=
ENST00000599899.5:n.1589+118T=
ENST00000601008.1:c.242-1049T=	ENSP00000471384.1:n.242-1049T=
ENST00000602229.1:c.77+118T=
NM_000064.3:c.4630+118T=	NP_000055.2:n.4630+118T=
NM_000064.4:c.4630+118T= MANE Select	NP_000055.2:n.4630+118T=