Canonical Allele Identifier: CA2320559110

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697552C= , CM000681.2:g.6697552C=	GRCh38
NC_000019.9:g.6697563C= , CM000681.1:g.6697563C=	GRCh37
NC_000019.8:g.6648563C=	NCBI36
NG_009557.1:g.28100G= , LRG_27:g.28100G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.936G=
ENST00000695652.1:c.2465G=	ENSP00000512083.1:p.Arg822=
ENST00000695653.1:c.497G=	ENSP00000512084.1:p.Arg166=
ENST00000695654.1:c.1712G=	ENSP00000512085.1:p.Arg571=
ENST00000695655.1:c.1529G=	ENSP00000512086.1:n.1529G=
ENST00000695692.1:n.1952G=
ENST00000245907.11:c.2588G= MANE Select	ENSP00000245907.4:p.Arg863=
ENST00000245907.10:c.2588G=	ENSP00000245907.4:p.Arg863=
ENST00000594005.1:n.164G=
NM_000064.3:c.2588G=	NP_000055.2:p.Arg863=
NM_000064.4:c.2588G= MANE Select	NP_000055.2:p.Arg863=