Canonical Allele Identifier: CA2320567922

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713427C= , CM000681.2:g.6713427C=	GRCh38
NC_000019.9:g.6713438C= , CM000681.1:g.6713438C=	GRCh37
NC_000019.8:g.6664438C=	NCBI36
NG_009557.1:g.12225G= , LRG_27:g.12225G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.733G=	ENSP00000512083.1:p.Glu245=
ENST00000695692.1:n.180G=
ENST00000245907.11:c.856G= MANE Select	ENSP00000245907.4:p.Glu286=
ENST00000245907.10:c.856G=	ENSP00000245907.4:p.Glu286=
ENST00000595577.1:n.360G=
ENST00000597442.5:n.106G=
NM_000064.3:c.856G=	NP_000055.2:p.Glu286=
NM_000064.4:c.856G= MANE Select	NP_000055.2:p.Glu286=