Canonical Allele Identifier: CA2320559211

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697753C= , CM000681.2:g.6697753C=	GRCh38
NC_000019.9:g.6697764C= , CM000681.1:g.6697764C=	GRCh37
NC_000019.8:g.6648764C=	NCBI36
NG_009557.1:g.27899G= , LRG_27:g.27899G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.830G=
ENST00000695652.1:c.2359G=	ENSP00000512083.1:p.Asp787=
ENST00000695653.1:c.391G=	ENSP00000512084.1:p.Asp131=
ENST00000695654.1:c.1606G=	ENSP00000512085.1:p.Asp536=
ENST00000695655.1:c.1423G=	ENSP00000512086.1:n.1423G=
ENST00000695692.1:n.1846G=
ENST00000245907.11:c.2482G= MANE Select	ENSP00000245907.4:p.Asp828=
ENST00000245907.10:c.2482G=	ENSP00000245907.4:p.Asp828=
ENST00000602053.1:n.530G=
NM_000064.3:c.2482G=	NP_000055.2:p.Asp828=
NM_000064.4:c.2482G= MANE Select	NP_000055.2:p.Asp828=