Canonical Allele Identifier: CA2320567862

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713295C= , CM000681.2:g.6713295C=	GRCh38
NC_000019.9:g.6713306C= , CM000681.1:g.6713306C=	GRCh37
NC_000019.8:g.6664306C=	NCBI36
NG_009557.1:g.12357G= , LRG_27:g.12357G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.774G=	ENSP00000512083.1:p.Glu258=
ENST00000695654.1:c.21G=	ENSP00000512085.1:p.Glu7=
ENST00000695692.1:n.221G=
ENST00000245907.11:c.897G= MANE Select	ENSP00000245907.4:p.Glu299=
ENST00000245907.10:c.897G=	ENSP00000245907.4:p.Glu299=
ENST00000594270.5:n.21G=
ENST00000595577.1:n.401G=
ENST00000597442.5:n.147G=
NM_000064.3:c.897G=	NP_000055.2:p.Glu299=
NM_000064.4:c.897G= MANE Select	NP_000055.2:p.Glu299=