Canonical Allele Identifier: CA2320553498

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686287T= , CM000681.2:g.6686287T=	GRCh38
NC_000019.9:g.6686298T= , CM000681.1:g.6686298T=	GRCh37
NC_000019.8:g.6637298T=	NCBI36
NG_009557.1:g.39365A= , LRG_27:g.39365A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1995A=
ENST00000695652.1:c.3524A=	ENSP00000512083.1:p.Asp1175=
ENST00000695653.1:c.1556A=	ENSP00000512084.1:p.Asp519=
ENST00000695654.1:c.2672A=	ENSP00000512085.1:p.Asp891=
ENST00000695655.1:c.2588A=	ENSP00000512086.1:n.2588A=
ENST00000695692.1:n.3011A=
ENST00000245907.11:c.3647A= MANE Select	ENSP00000245907.4:p.Asp1216=
ENST00000245907.10:c.3647A=	ENSP00000245907.4:p.Asp1216=
ENST00000596238.1:n.90A=
ENST00000601008.1:c.241+459A=	ENSP00000471384.1:n.241+459A=
NM_000064.3:c.3647A=	NP_000055.2:p.Asp1216=
NM_000064.4:c.3647A= MANE Select	NP_000055.2:p.Asp1216=