Canonical Allele Identifier: CA2320559172

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697672G= , CM000681.2:g.6697672G=	GRCh38
NC_000019.9:g.6697683G= , CM000681.1:g.6697683G=	GRCh37
NC_000019.8:g.6648683G=	NCBI36
NG_009557.1:g.27980C= , LRG_27:g.27980C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.911C=
ENST00000695652.1:c.2440C=	ENSP00000512083.1:p.Arg814=
ENST00000695653.1:c.472C=	ENSP00000512084.1:p.Arg158=
ENST00000695654.1:c.1687C=	ENSP00000512085.1:p.Arg563=
ENST00000695655.1:c.1504C=	ENSP00000512086.1:n.1504C=
ENST00000695692.1:n.1927C=
ENST00000245907.11:c.2563C= MANE Select	ENSP00000245907.4:p.Arg855=
ENST00000245907.10:c.2563C=	ENSP00000245907.4:p.Arg855=
ENST00000594005.1:n.44C=
ENST00000602053.1:n.611C=
NM_000064.3:c.2563C=	NP_000055.2:p.Arg855=
NM_000064.4:c.2563C= MANE Select	NP_000055.2:p.Arg855=