Canonical Allele Identifier: CA2320553494

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686271C= , CM000681.2:g.6686271C=	GRCh38
NC_000019.9:g.6686282C= , CM000681.1:g.6686282C=	GRCh37
NC_000019.8:g.6637282C=	NCBI36
NG_009557.1:g.39381G= , LRG_27:g.39381G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2011G=
ENST00000695652.1:c.3540G=	ENSP00000512083.1:p.Glu1180=
ENST00000695653.1:c.1572G=	ENSP00000512084.1:p.Glu524=
ENST00000695654.1:c.2688G=	ENSP00000512085.1:p.Glu896=
ENST00000695655.1:c.2604G=	ENSP00000512086.1:n.2604G=
ENST00000695692.1:n.3027G=
ENST00000245907.11:c.3663G= MANE Select	ENSP00000245907.4:p.Glu1221=
ENST00000245907.10:c.3663G=	ENSP00000245907.4:p.Glu1221=
ENST00000596238.1:n.106G=
ENST00000601008.1:c.241+475G=	ENSP00000471384.1:n.241+475G=
NM_000064.3:c.3663G=	NP_000055.2:p.Glu1221=
NM_000064.4:c.3663G= MANE Select	NP_000055.2:p.Glu1221=