Canonical Allele Identifier: CA2320559095

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697500C= , CM000681.2:g.6697500C=	GRCh38
NC_000019.9:g.6697511C= , CM000681.1:g.6697511C=	GRCh37
NC_000019.8:g.6648511C=	NCBI36
NG_009557.1:g.28152G= , LRG_27:g.28152G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.988G=
ENST00000695652.1:c.2517G=	ENSP00000512083.1:p.Arg839=
ENST00000695653.1:c.549G=	ENSP00000512084.1:p.Arg183=
ENST00000695654.1:c.1764G=	ENSP00000512085.1:p.Arg588=
ENST00000695655.1:c.1581G=	ENSP00000512086.1:n.1581G=
ENST00000695692.1:n.2004G=
ENST00000245907.11:c.2640G= MANE Select	ENSP00000245907.4:p.Arg880=
ENST00000245907.10:c.2640G=	ENSP00000245907.4:p.Arg880=
ENST00000594005.1:n.216G=
NM_000064.3:c.2640G=	NP_000055.2:p.Arg880=
NM_000064.4:c.2640G= MANE Select	NP_000055.2:p.Arg880=