Canonical Allele Identifier: CA2320559062

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697442T= , CM000681.2:g.6697442T=	GRCh38
NC_000019.9:g.6697453T= , CM000681.1:g.6697453T=	GRCh37
NC_000019.8:g.6648453T=	NCBI36
NG_009557.1:g.28210A= , LRG_27:g.28210A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1046A=
ENST00000695652.1:c.2575A=	ENSP00000512083.1:p.Ile859=
ENST00000695653.1:c.607A=	ENSP00000512084.1:p.Ile203=
ENST00000695654.1:c.1822A=	ENSP00000512085.1:p.Ile608=
ENST00000695655.1:c.1639A=	ENSP00000512086.1:n.1639A=
ENST00000695692.1:n.2062A=
ENST00000245907.11:c.2698A= MANE Select	ENSP00000245907.4:p.Ile900=
ENST00000245907.10:c.2698A=	ENSP00000245907.4:p.Ile900=
ENST00000594005.1:n.274A=
NM_000064.3:c.2698A=	NP_000055.2:p.Ile900=
NM_000064.4:c.2698A= MANE Select	NP_000055.2:p.Ile900=