Canonical Allele Identifier: CA2320559039

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697358A= , CM000681.2:g.6697358A=	GRCh38
NC_000019.9:g.6697369A= , CM000681.1:g.6697369A=	GRCh37
NC_000019.8:g.6648369A=	NCBI36
NG_009557.1:g.28294T= , LRG_27:g.28294T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1130T=
ENST00000695652.1:c.2659T=	ENSP00000512083.1:p.Ser887=
ENST00000695653.1:c.691T=	ENSP00000512084.1:p.Ser231=
ENST00000695654.1:c.1906T=	ENSP00000512085.1:p.Ser636=
ENST00000695655.1:c.1723T=	ENSP00000512086.1:n.1723T=
ENST00000695692.1:n.2146T=
ENST00000245907.11:c.2782T= MANE Select	ENSP00000245907.4:p.Ser928=
ENST00000245907.10:c.2782T=	ENSP00000245907.4:p.Ser928=
ENST00000594005.1:n.358T=
NM_000064.3:c.2782T=	NP_000055.2:p.Ser928=
NM_000064.4:c.2782T= MANE Select	NP_000055.2:p.Ser928=