Canonical Allele Identifier: CA2320550289

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679187G= , CM000681.2:g.6679187G=	GRCh38
NC_000019.9:g.6679198G= , CM000681.1:g.6679198G=	GRCh37
NC_000019.8:g.6630198G=	NCBI36
NG_009557.1:g.46465C= , LRG_27:g.46465C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2916C=
ENST00000695653.1:c.2477C=	ENSP00000512084.1:p.Ser826=
ENST00000695654.1:c.3593C=	ENSP00000512085.1:p.Ser1198=
ENST00000695689.1:c.539C=	ENSP00000512101.1:n.539C=
ENST00000695690.1:n.1633C=
ENST00000695691.1:n.1429C=
ENST00000245907.11:c.4568C= MANE Select	ENSP00000245907.4:p.Ser1523=
ENST00000245907.10:c.4568C=	ENSP00000245907.4:p.Ser1523=
ENST00000599668.1:n.188C=
ENST00000599899.5:n.1527C=
ENST00000601008.1:c.242-1229C=	ENSP00000471384.1:n.242-1229C=
ENST00000602229.1:c.15C=
NM_000064.3:c.4568C=	NP_000055.2:p.Ser1523=
NM_000064.4:c.4568C= MANE Select	NP_000055.2:p.Ser1523=