Canonical Allele Identifier: CA2320559188

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697704T= , CM000681.2:g.6697704T=	GRCh38
NC_000019.9:g.6697715T= , CM000681.1:g.6697715T=	GRCh37
NC_000019.8:g.6648715T=	NCBI36
NG_009557.1:g.27948A= , LRG_27:g.27948A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.879A=
ENST00000695652.1:c.2408A=	ENSP00000512083.1:p.Gln803=
ENST00000695653.1:c.440A=	ENSP00000512084.1:p.Gln147=
ENST00000695654.1:c.1655A=	ENSP00000512085.1:p.Gln552=
ENST00000695655.1:c.1472A=	ENSP00000512086.1:n.1472A=
ENST00000695692.1:n.1895A=
ENST00000245907.11:c.2531A= MANE Select	ENSP00000245907.4:p.Gln844=
ENST00000245907.10:c.2531A=	ENSP00000245907.4:p.Gln844=
ENST00000594005.1:n.12A=
ENST00000602053.1:n.579A=
NM_000064.3:c.2531A=	NP_000055.2:p.Gln844=
NM_000064.4:c.2531A= MANE Select	NP_000055.2:p.Gln844=