Canonical Allele Identifier: CA2320559064

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697446A= , CM000681.2:g.6697446A=	GRCh38
NC_000019.9:g.6697457A= , CM000681.1:g.6697457A=	GRCh37
NC_000019.8:g.6648457A=	NCBI36
NG_009557.1:g.28206T= , LRG_27:g.28206T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1042T=
ENST00000695652.1:c.2571T=	ENSP00000512083.1:p.Tyr857=
ENST00000695653.1:c.603T=	ENSP00000512084.1:p.Tyr201=
ENST00000695654.1:c.1818T=	ENSP00000512085.1:p.Tyr606=
ENST00000695655.1:c.1635T=	ENSP00000512086.1:n.1635T=
ENST00000695692.1:n.2058T=
ENST00000245907.11:c.2694T= MANE Select	ENSP00000245907.4:p.Tyr898=
ENST00000245907.10:c.2694T=	ENSP00000245907.4:p.Tyr898=
ENST00000594005.1:n.270T=
NM_000064.3:c.2694T=	NP_000055.2:p.Tyr898=
NM_000064.4:c.2694T= MANE Select	NP_000055.2:p.Tyr898=