Canonical Allele Identifier: CA2320553452

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686173C= , CM000681.2:g.6686173C=	GRCh38
NC_000019.9:g.6686184C= , CM000681.1:g.6686184C=	GRCh37
NC_000019.8:g.6637184C=	NCBI36
NG_009557.1:g.39479G= , LRG_27:g.39479G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2109G=
ENST00000695652.1:c.3638G=	ENSP00000512083.1:p.Arg1213=
ENST00000695653.1:c.1670G=	ENSP00000512084.1:p.Arg557=
ENST00000695654.1:c.2786G=	ENSP00000512085.1:p.Arg929=
ENST00000695655.1:c.2702G=	ENSP00000512086.1:n.2702G=
ENST00000695692.1:n.3125G=
ENST00000245907.11:c.3761G= MANE Select	ENSP00000245907.4:p.Arg1254=
ENST00000245907.10:c.3761G=	ENSP00000245907.4:p.Arg1254=
ENST00000596238.1:n.204G=
ENST00000601008.1:c.241+573G=	ENSP00000471384.1:n.241+573G=
NM_000064.3:c.3761G=	NP_000055.2:p.Arg1254=
NM_000064.4:c.3761G= MANE Select	NP_000055.2:p.Arg1254=