Canonical Allele Identifier: CA2320550218

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679016A= , CM000681.2:g.6679016A=	GRCh38
NC_000019.9:g.6679027A= , CM000681.1:g.6679027A=	GRCh37
NC_000019.8:g.6630027A=	NCBI36
NG_009557.1:g.46636T= , LRG_27:g.46636T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2978+109T=
ENST00000695653.1:c.2539+109T=	ENSP00000512084.1:n.2539+109T=
ENST00000695654.1:c.3655+109T=	ENSP00000512085.1:n.3655+109T=
ENST00000695689.1:c.601+109T=	ENSP00000512101.1:n.601+109T=
ENST00000695690.1:n.1695+109T=
ENST00000695691.1:n.1491+109T=
ENST00000245907.11:c.4630+109T= MANE Select	ENSP00000245907.4:n.4630+109T=
ENST00000245907.10:c.4630+109T=	ENSP00000245907.4:n.4630+109T=
ENST00000599668.1:n.250+109T=
ENST00000599899.5:n.1589+109T=
ENST00000601008.1:c.242-1058T=	ENSP00000471384.1:n.242-1058T=
ENST00000602229.1:c.77+109T=
NM_000064.3:c.4630+109T=	NP_000055.2:n.4630+109T=
NM_000064.4:c.4630+109T= MANE Select	NP_000055.2:n.4630+109T=