Canonical Allele Identifier: CA2320553462

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686193G= , CM000681.2:g.6686193G=	GRCh38
NC_000019.9:g.6686204G= , CM000681.1:g.6686204G=	GRCh37
NC_000019.8:g.6637204G=	NCBI36
NG_009557.1:g.39459C= , LRG_27:g.39459C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2089C=
ENST00000695652.1:c.3618C=	ENSP00000512083.1:p.Asp1206=
ENST00000695653.1:c.1650C=	ENSP00000512084.1:p.Asp550=
ENST00000695654.1:c.2766C=	ENSP00000512085.1:p.Asp922=
ENST00000695655.1:c.2682C=	ENSP00000512086.1:n.2682C=
ENST00000695692.1:n.3105C=
ENST00000245907.11:c.3741C= MANE Select	ENSP00000245907.4:p.Asp1247=
ENST00000245907.10:c.3741C=	ENSP00000245907.4:p.Asp1247=
ENST00000596238.1:n.184C=
ENST00000601008.1:c.241+553C=	ENSP00000471384.1:n.241+553C=
NM_000064.3:c.3741C=	NP_000055.2:p.Asp1247=
NM_000064.4:c.3741C= MANE Select	NP_000055.2:p.Asp1247=