Canonical Allele Identifier: CA2320559180

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697689G= , CM000681.2:g.6697689G=	GRCh38
NC_000019.9:g.6697700G= , CM000681.1:g.6697700G=	GRCh37
NC_000019.8:g.6648700G=	NCBI36
NG_009557.1:g.27963C= , LRG_27:g.27963C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.894C=
ENST00000695652.1:c.2423C=	ENSP00000512083.1:p.Ala808=
ENST00000695653.1:c.455C=	ENSP00000512084.1:p.Ala152=
ENST00000695654.1:c.1670C=	ENSP00000512085.1:p.Ala557=
ENST00000695655.1:c.1487C=	ENSP00000512086.1:n.1487C=
ENST00000695692.1:n.1910C=
ENST00000245907.11:c.2546C= MANE Select	ENSP00000245907.4:p.Ala849=
ENST00000245907.10:c.2546C=	ENSP00000245907.4:p.Ala849=
ENST00000594005.1:n.27C=
ENST00000602053.1:n.594C=
NM_000064.3:c.2546C=	NP_000055.2:p.Ala849=
NM_000064.4:c.2546C= MANE Select	NP_000055.2:p.Ala849=