Canonical Allele Identifier: CA2320550441

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679489G= , CM000681.2:g.6679489G=	GRCh38
NC_000019.9:g.6679500G= , CM000681.1:g.6679500G=	GRCh37
NC_000019.8:g.6630500G=	NCBI36
NG_009557.1:g.46163C= , LRG_27:g.46163C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2812C=
ENST00000695653.1:c.2373C=	ENSP00000512084.1:p.Ser791=
ENST00000695654.1:c.3489C=	ENSP00000512085.1:p.Ser1163=
ENST00000695689.1:c.435C=	ENSP00000512101.1:n.435C=
ENST00000695690.1:n.1529C=
ENST00000695691.1:n.1325C=
ENST00000245907.11:c.4464C= MANE Select	ENSP00000245907.4:p.Ser1488=
ENST00000245907.10:c.4464C=	ENSP00000245907.4:p.Ser1488=
ENST00000599668.1:n.59C=
ENST00000599899.5:n.1423C=
ENST00000601008.1:c.242-1531C=	ENSP00000471384.1:n.242-1531C=
NM_000064.3:c.4464C=	NP_000055.2:p.Ser1488=
NM_000064.4:c.4464C= MANE Select	NP_000055.2:p.Ser1488=