Canonical Allele Identifier: CA2320553496

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686279G= , CM000681.2:g.6686279G=	GRCh38
NC_000019.9:g.6686290G= , CM000681.1:g.6686290G=	GRCh37
NC_000019.8:g.6637290G=	NCBI36
NG_009557.1:g.39373C= , LRG_27:g.39373C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2003C=
ENST00000695652.1:c.3532C=	ENSP00000512083.1:p.Arg1178=
ENST00000695653.1:c.1564C=	ENSP00000512084.1:p.Arg522=
ENST00000695654.1:c.2680C=	ENSP00000512085.1:p.Arg894=
ENST00000695655.1:c.2596C=	ENSP00000512086.1:n.2596C=
ENST00000695692.1:n.3019C=
ENST00000245907.11:c.3655C= MANE Select	ENSP00000245907.4:p.Arg1219=
ENST00000245907.10:c.3655C=	ENSP00000245907.4:p.Arg1219=
ENST00000596238.1:n.98C=
ENST00000601008.1:c.241+467C=	ENSP00000471384.1:n.241+467C=
NM_000064.3:c.3655C=	NP_000055.2:p.Arg1219=
NM_000064.4:c.3655C= MANE Select	NP_000055.2:p.Arg1219=