Canonical Allele Identifier: CA2320559171

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697671C= , CM000681.2:g.6697671C=	GRCh38
NC_000019.9:g.6697682C= , CM000681.1:g.6697682C=	GRCh37
NC_000019.8:g.6648682C=	NCBI36
NG_009557.1:g.27981G= , LRG_27:g.27981G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.912G=
ENST00000695652.1:c.2441G=	ENSP00000512083.1:p.Arg814=
ENST00000695653.1:c.473G=	ENSP00000512084.1:p.Arg158=
ENST00000695654.1:c.1688G=	ENSP00000512085.1:p.Arg563=
ENST00000695655.1:c.1505G=	ENSP00000512086.1:n.1505G=
ENST00000695692.1:n.1928G=
ENST00000245907.11:c.2564G= MANE Select	ENSP00000245907.4:p.Arg855=
ENST00000245907.10:c.2564G=	ENSP00000245907.4:p.Arg855=
ENST00000594005.1:n.45G=
ENST00000602053.1:n.612G=
NM_000064.3:c.2564G=	NP_000055.2:p.Arg855=
NM_000064.4:c.2564G= MANE Select	NP_000055.2:p.Arg855=