Canonical Allele Identifier: CA2320551542

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6681973C= , CM000681.2:g.6681973C=	GRCh38
NC_000019.9:g.6681984C= , CM000681.1:g.6681984C=	GRCh37
NC_000019.8:g.6632984C=	NCBI36
NG_009557.1:g.43679G= , LRG_27:g.43679G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2666G=
ENST00000695653.1:c.2227G=	ENSP00000512084.1:p.Asp743=
ENST00000695654.1:c.3343G=	ENSP00000512085.1:p.Asp1115=
ENST00000695689.1:c.289G=	ENSP00000512101.1:n.289G=
ENST00000695690.1:n.509G=
ENST00000695691.1:n.509G=
ENST00000245907.11:c.4318G= MANE Select	ENSP00000245907.4:p.Asp1440=
ENST00000245907.10:c.4318G=	ENSP00000245907.4:p.Asp1440=
ENST00000596548.1:c.439G=	ENSP00000469744.1:p.Asp147=
ENST00000599899.5:n.1277G=
ENST00000601008.1:c.242-4015G=	ENSP00000471384.1:n.242-4015G=
NM_000064.3:c.4318G=	NP_000055.2:p.Asp1440=
NM_000064.4:c.4318G= MANE Select	NP_000055.2:p.Asp1440=