Canonical Allele Identifier: CA2320553495

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686278C= , CM000681.2:g.6686278C=	GRCh38
NC_000019.9:g.6686289C= , CM000681.1:g.6686289C=	GRCh37
NC_000019.8:g.6637289C=	NCBI36
NG_009557.1:g.39374G= , LRG_27:g.39374G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2004G=
ENST00000695652.1:c.3533G=	ENSP00000512083.1:p.Arg1178=
ENST00000695653.1:c.1565G=	ENSP00000512084.1:p.Arg522=
ENST00000695654.1:c.2681G=	ENSP00000512085.1:p.Arg894=
ENST00000695655.1:c.2597G=	ENSP00000512086.1:n.2597G=
ENST00000695692.1:n.3020G=
ENST00000245907.11:c.3656G= MANE Select	ENSP00000245907.4:p.Arg1219=
ENST00000245907.10:c.3656G=	ENSP00000245907.4:p.Arg1219=
ENST00000596238.1:n.99G=
ENST00000601008.1:c.241+468G=	ENSP00000471384.1:n.241+468G=
NM_000064.3:c.3656G=	NP_000055.2:p.Arg1219=
NM_000064.4:c.3656G= MANE Select	NP_000055.2:p.Arg1219=