Canonical Allele Identifier: CA2320559174

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697675A= , CM000681.2:g.6697675A=	GRCh38
NC_000019.9:g.6697686A= , CM000681.1:g.6697686A=	GRCh37
NC_000019.8:g.6648686A=	NCBI36
NG_009557.1:g.27977T= , LRG_27:g.27977T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.908T=
ENST00000695652.1:c.2437T=	ENSP00000512083.1:p.Tyr813=
ENST00000695653.1:c.469T=	ENSP00000512084.1:p.Tyr157=
ENST00000695654.1:c.1684T=	ENSP00000512085.1:p.Tyr562=
ENST00000695655.1:c.1501T=	ENSP00000512086.1:n.1501T=
ENST00000695692.1:n.1924T=
ENST00000245907.11:c.2560T= MANE Select	ENSP00000245907.4:p.Tyr854=
ENST00000245907.10:c.2560T=	ENSP00000245907.4:p.Tyr854=
ENST00000594005.1:n.41T=
ENST00000602053.1:n.608T=
NM_000064.3:c.2560T=	NP_000055.2:p.Tyr854=
NM_000064.4:c.2560T= MANE Select	NP_000055.2:p.Tyr854=