Canonical Allele Identifier: CA2320553486

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686251T= , CM000681.2:g.6686251T=	GRCh38
NC_000019.9:g.6686262T= , CM000681.1:g.6686262T=	GRCh37
NC_000019.8:g.6637262T=	NCBI36
NG_009557.1:g.39401A= , LRG_27:g.39401A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2031A=
ENST00000695652.1:c.3560A=	ENSP00000512083.1:p.Tyr1187=
ENST00000695653.1:c.1592A=	ENSP00000512084.1:p.Tyr531=
ENST00000695654.1:c.2708A=	ENSP00000512085.1:p.Tyr903=
ENST00000695655.1:c.2624A=	ENSP00000512086.1:n.2624A=
ENST00000695692.1:n.3047A=
ENST00000245907.11:c.3683A= MANE Select	ENSP00000245907.4:p.Tyr1228=
ENST00000245907.10:c.3683A=	ENSP00000245907.4:p.Tyr1228=
ENST00000596238.1:n.126A=
ENST00000601008.1:c.241+495A=	ENSP00000471384.1:n.241+495A=
NM_000064.3:c.3683A=	NP_000055.2:p.Tyr1228=
NM_000064.4:c.3683A= MANE Select	NP_000055.2:p.Tyr1228=