Canonical Allele Identifier: CA2320550416

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679428C= , CM000681.2:g.6679428C=	GRCh38
NC_000019.9:g.6679439C= , CM000681.1:g.6679439C=	GRCh37
NC_000019.8:g.6630439C=	NCBI36
NG_009557.1:g.46224G= , LRG_27:g.46224G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2873G=
ENST00000695653.1:c.2434G=	ENSP00000512084.1:p.Glu812=
ENST00000695654.1:c.3550G=	ENSP00000512085.1:p.Glu1184=
ENST00000695689.1:c.496G=	ENSP00000512101.1:n.496G=
ENST00000695690.1:n.1590G=
ENST00000695691.1:n.1386G=
ENST00000245907.11:c.4525G= MANE Select	ENSP00000245907.4:p.Glu1509=
ENST00000245907.10:c.4525G=	ENSP00000245907.4:p.Glu1509=
ENST00000599668.1:n.120G=
ENST00000599899.5:n.1484G=
ENST00000601008.1:c.242-1470G=	ENSP00000471384.1:n.242-1470G=
NM_000064.3:c.4525G=	NP_000055.2:p.Glu1509=
NM_000064.4:c.4525G= MANE Select	NP_000055.2:p.Glu1509=