Canonical Allele Identifier: CA2320559224

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697792T= , CM000681.2:g.6697792T=	GRCh38
NC_000019.9:g.6697803T= , CM000681.1:g.6697803T=	GRCh37
NC_000019.8:g.6648803T=	NCBI36
NG_009557.1:g.27860A= , LRG_27:g.27860A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.791A=
ENST00000695652.1:c.2320A=	ENSP00000512083.1:p.Ile774=
ENST00000695653.1:c.352A=	ENSP00000512084.1:p.Ile118=
ENST00000695654.1:c.1567A=	ENSP00000512085.1:p.Ile523=
ENST00000695655.1:c.1384A=	ENSP00000512086.1:n.1384A=
ENST00000695692.1:n.1807A=
ENST00000245907.11:c.2443A= MANE Select	ENSP00000245907.4:p.Ile815=
ENST00000245907.10:c.2443A=	ENSP00000245907.4:p.Ile815=
ENST00000602053.1:n.491A=
NM_000064.3:c.2443A=	NP_000055.2:p.Ile815=
NM_000064.4:c.2443A= MANE Select	NP_000055.2:p.Ile815=