Canonical Allele Identifier: CA2320567931

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713447T= , CM000681.2:g.6713447T=	GRCh38
NC_000019.9:g.6713458T= , CM000681.1:g.6713458T=	GRCh37
NC_000019.8:g.6664458T=	NCBI36
NG_009557.1:g.12205A= , LRG_27:g.12205A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.713A=	ENSP00000512083.1:p.Glu238=
ENST00000695692.1:n.160A=
ENST00000245907.11:c.836A= MANE Select	ENSP00000245907.4:p.Glu279=
ENST00000245907.10:c.836A=	ENSP00000245907.4:p.Glu279=
ENST00000595577.1:n.340A=
ENST00000597442.5:n.86A=
NM_000064.3:c.836A=	NP_000055.2:p.Glu279=
NM_000064.4:c.836A= MANE Select	NP_000055.2:p.Glu279=