Canonical Allele Identifier: CA2320556794

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6692971C= , CM000681.2:g.6692971C=	GRCh38
NC_000019.9:g.6692982C= , CM000681.1:g.6692982C=	GRCh37
NC_000019.8:g.6643982C=	NCBI36
NG_009557.1:g.32681G= , LRG_27:g.32681G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000064.4:c.3343G= MANE Select	NP_000055.2:p.Asp1115=
ENST00000245907.11:c.3343G= MANE Select	ENSP00000245907.4:p.Asp1115=
NM_000064.3:c.3343G=	NP_000055.2:p.Asp1115=
ENST00000245907.10:c.3343G=	ENSP00000245907.4:p.Asp1115=
ENST00000598805.2:n.113G=
ENST00000695651.1:n.1691G=
ENST00000695652.1:c.3220G=	ENSP00000512083.1:p.Asp1074=
ENST00000695653.1:c.1252G=	ENSP00000512084.1:p.Asp418=
ENST00000695654.1:c.2467G=	ENSP00000512085.1:p.Asp823=
ENST00000695655.1:c.2284G=	ENSP00000512086.1:n.2284G=
ENST00000695692.1:n.2707G=