Canonical Allele Identifier: CA2320567823

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713213A= , CM000681.2:g.6713213A=	GRCh38
NC_000019.9:g.6713224A= , CM000681.1:g.6713224A=	GRCh37
NC_000019.8:g.6664224A=	NCBI36
NG_009557.1:g.12439T= , LRG_27:g.12439T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.856T=	ENSP00000512083.1:p.Ser286=
ENST00000695654.1:c.103T=	ENSP00000512085.1:p.Ser35=
ENST00000695692.1:n.303T=
ENST00000245907.11:c.979T= MANE Select	ENSP00000245907.4:p.Ser327=
ENST00000245907.10:c.979T=	ENSP00000245907.4:p.Ser327=
ENST00000594270.5:n.103T=
ENST00000595577.1:n.483T=
ENST00000597442.5:n.229T=
NM_000064.3:c.979T=	NP_000055.2:p.Ser327=
NM_000064.4:c.979T= MANE Select	NP_000055.2:p.Ser327=