Canonical Allele Identifier: CA2320553444

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686145A= , CM000681.2:g.6686145A=	GRCh38
NC_000019.9:g.6686156A= , CM000681.1:g.6686156A=	GRCh37
NC_000019.8:g.6637156A=	NCBI36
NG_009557.1:g.39507T= , LRG_27:g.39507T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2137T=
ENST00000695652.1:c.3666T=	ENSP00000512083.1:p.Gly1222=
ENST00000695653.1:c.1698T=	ENSP00000512084.1:p.Gly566=
ENST00000695654.1:c.2814T=	ENSP00000512085.1:p.Gly938=
ENST00000695655.1:c.2730T=	ENSP00000512086.1:n.2730T=
ENST00000695692.1:n.3153T=
ENST00000245907.11:c.3789T= MANE Select	ENSP00000245907.4:p.Gly1263=
ENST00000245907.10:c.3789T=	ENSP00000245907.4:p.Gly1263=
ENST00000596238.1:n.232T=
ENST00000601008.1:c.241+601T=	ENSP00000471384.1:n.241+601T=
NM_000064.3:c.3789T=	NP_000055.2:p.Gly1263=
NM_000064.4:c.3789T= MANE Select	NP_000055.2:p.Gly1263=