Canonical Allele Identifier: CA2320559201

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697732G= , CM000681.2:g.6697732G=	GRCh38
NC_000019.9:g.6697743G= , CM000681.1:g.6697743G=	GRCh37
NC_000019.8:g.6648743G=	NCBI36
NG_009557.1:g.27920C= , LRG_27:g.27920C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.851C=
ENST00000695652.1:c.2380C=	ENSP00000512083.1:p.Leu794=
ENST00000695653.1:c.412C=	ENSP00000512084.1:p.Leu138=
ENST00000695654.1:c.1627C=	ENSP00000512085.1:p.Leu543=
ENST00000695655.1:c.1444C=	ENSP00000512086.1:n.1444C=
ENST00000695692.1:n.1867C=
ENST00000245907.11:c.2503C= MANE Select	ENSP00000245907.4:p.Leu835=
ENST00000245907.10:c.2503C=	ENSP00000245907.4:p.Leu835=
ENST00000602053.1:n.551C=
NM_000064.3:c.2503C=	NP_000055.2:p.Leu835=
NM_000064.4:c.2503C= MANE Select	NP_000055.2:p.Leu835=