Canonical Allele Identifier: CA2320551534

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6681953G= , CM000681.2:g.6681953G=	GRCh38
NC_000019.9:g.6681964G= , CM000681.1:g.6681964G=	GRCh37
NC_000019.8:g.6632964G=	NCBI36
NG_009557.1:g.43699C= , LRG_27:g.43699C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2686C=
ENST00000695653.1:c.2247C=	ENSP00000512084.1:p.Ile749=
ENST00000695654.1:c.3363C=	ENSP00000512085.1:p.Ile1121=
ENST00000695689.1:c.309C=	ENSP00000512101.1:n.309C=
ENST00000695690.1:n.529C=
ENST00000695691.1:n.529C=
ENST00000245907.11:c.4338C= MANE Select	ENSP00000245907.4:p.Ile1446=
ENST00000245907.10:c.4338C=	ENSP00000245907.4:p.Ile1446=
ENST00000596548.1:c.459C=	ENSP00000469744.1:p.Ile153=
ENST00000599899.5:n.1297C=
ENST00000601008.1:c.242-3995C=	ENSP00000471384.1:n.242-3995C=
NM_000064.3:c.4338C=	NP_000055.2:p.Ile1446=
NM_000064.4:c.4338C= MANE Select	NP_000055.2:p.Ile1446=