Canonical Allele Identifier: CA2320559191

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697713C= , CM000681.2:g.6697713C=	GRCh38
NC_000019.9:g.6697724C= , CM000681.1:g.6697724C=	GRCh37
NC_000019.8:g.6648724C=	NCBI36
NG_009557.1:g.27939G= , LRG_27:g.27939G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.870G=
ENST00000695652.1:c.2399G=	ENSP00000512083.1:p.Arg800=
ENST00000695653.1:c.431G=	ENSP00000512084.1:p.Arg144=
ENST00000695654.1:c.1646G=	ENSP00000512085.1:p.Arg549=
ENST00000695655.1:c.1463G=	ENSP00000512086.1:n.1463G=
ENST00000695692.1:n.1886G=
ENST00000245907.11:c.2522G= MANE Select	ENSP00000245907.4:p.Arg841=
ENST00000245907.10:c.2522G=	ENSP00000245907.4:p.Arg841=
ENST00000594005.1:n.3G=
ENST00000602053.1:n.570G=
NM_000064.3:c.2522G=	NP_000055.2:p.Arg841=
NM_000064.4:c.2522G= MANE Select	NP_000055.2:p.Arg841=