Canonical Allele Identifier: CA2320559203

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697734C= , CM000681.2:g.6697734C=	GRCh38
NC_000019.9:g.6697745C= , CM000681.1:g.6697745C=	GRCh37
NC_000019.8:g.6648745C=	NCBI36
NG_009557.1:g.27918G= , LRG_27:g.27918G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.849G=
ENST00000695652.1:c.2378G=	ENSP00000512083.1:p.Arg793=
ENST00000695653.1:c.410G=	ENSP00000512084.1:p.Arg137=
ENST00000695654.1:c.1625G=	ENSP00000512085.1:p.Arg542=
ENST00000695655.1:c.1442G=	ENSP00000512086.1:n.1442G=
ENST00000695692.1:n.1865G=
ENST00000245907.11:c.2501G= MANE Select	ENSP00000245907.4:p.Arg834=
ENST00000245907.10:c.2501G=	ENSP00000245907.4:p.Arg834=
ENST00000602053.1:n.549G=
NM_000064.3:c.2501G=	NP_000055.2:p.Arg834=
NM_000064.4:c.2501G= MANE Select	NP_000055.2:p.Arg834=