Canonical Allele Identifier: CA2320551549

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6681988C= , CM000681.2:g.6681988C=	GRCh38
NC_000019.9:g.6681999C= , CM000681.1:g.6681999C=	GRCh37
NC_000019.8:g.6632999C=	NCBI36
NG_009557.1:g.43664G= , LRG_27:g.43664G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2651G=
ENST00000695653.1:c.2212G=	ENSP00000512084.1:p.Asp738=
ENST00000695654.1:c.3328G=	ENSP00000512085.1:p.Asp1110=
ENST00000695689.1:c.274G=	ENSP00000512101.1:n.274G=
ENST00000695690.1:n.494G=
ENST00000695691.1:n.494G=
ENST00000245907.11:c.4303G= MANE Select	ENSP00000245907.4:p.Asp1435=
ENST00000245907.10:c.4303G=	ENSP00000245907.4:p.Asp1435=
ENST00000596548.1:c.424G=	ENSP00000469744.1:p.Asp142=
ENST00000599899.5:n.1262G=
ENST00000601008.1:c.242-4030G=	ENSP00000471384.1:n.242-4030G=
NM_000064.3:c.4303G=	NP_000055.2:p.Asp1435=
NM_000064.4:c.4303G= MANE Select	NP_000055.2:p.Asp1435=