Canonical Allele Identifier: CA2320553497

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686283C= , CM000681.2:g.6686283C=	GRCh38
NC_000019.9:g.6686294C= , CM000681.1:g.6686294C=	GRCh37
NC_000019.8:g.6637294C=	NCBI36
NG_009557.1:g.39369G= , LRG_27:g.39369G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1999G=
ENST00000695652.1:c.3528G=	ENSP00000512083.1:p.Lys1176=
ENST00000695653.1:c.1560G=	ENSP00000512084.1:p.Lys520=
ENST00000695654.1:c.2676G=	ENSP00000512085.1:p.Lys892=
ENST00000695655.1:c.2592G=	ENSP00000512086.1:n.2592G=
ENST00000695692.1:n.3015G=
ENST00000245907.11:c.3651G= MANE Select	ENSP00000245907.4:p.Lys1217=
ENST00000245907.10:c.3651G=	ENSP00000245907.4:p.Lys1217=
ENST00000596238.1:n.94G=
ENST00000601008.1:c.241+463G=	ENSP00000471384.1:n.241+463G=
NM_000064.3:c.3651G=	NP_000055.2:p.Lys1217=
NM_000064.4:c.3651G= MANE Select	NP_000055.2:p.Lys1217=