Canonical Allele Identifier: CA2320559209

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697747A= , CM000681.2:g.6697747A=	GRCh38
NC_000019.9:g.6697758A= , CM000681.1:g.6697758A=	GRCh37
NC_000019.8:g.6648758A=	NCBI36
NG_009557.1:g.27905T= , LRG_27:g.27905T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.836T=
ENST00000695652.1:c.2365T=	ENSP00000512083.1:p.Phe789=
ENST00000695653.1:c.397T=	ENSP00000512084.1:p.Phe133=
ENST00000695654.1:c.1612T=	ENSP00000512085.1:p.Phe538=
ENST00000695655.1:c.1429T=	ENSP00000512086.1:n.1429T=
ENST00000695692.1:n.1852T=
ENST00000245907.11:c.2488T= MANE Select	ENSP00000245907.4:p.Phe830=
ENST00000245907.10:c.2488T=	ENSP00000245907.4:p.Phe830=
ENST00000602053.1:n.536T=
NM_000064.3:c.2488T=	NP_000055.2:p.Phe830=
NM_000064.4:c.2488T= MANE Select	NP_000055.2:p.Phe830=