Canonical Allele Identifier: CA2320567929

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713442T= , CM000681.2:g.6713442T=	GRCh38
NC_000019.9:g.6713453T= , CM000681.1:g.6713453T=	GRCh37
NC_000019.8:g.6664453T=	NCBI36
NG_009557.1:g.12210A= , LRG_27:g.12210A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.718A=	ENSP00000512083.1:p.Arg240=
ENST00000695692.1:n.165A=
ENST00000245907.11:c.841A= MANE Select	ENSP00000245907.4:p.Arg281=
ENST00000245907.10:c.841A=	ENSP00000245907.4:p.Arg281=
ENST00000595577.1:n.345A=
ENST00000597442.5:n.91A=
NM_000064.3:c.841A=	NP_000055.2:p.Arg281=
NM_000064.4:c.841A= MANE Select	NP_000055.2:p.Arg281=