Canonical Allele Identifier: CA2320551547

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6681981G= , CM000681.2:g.6681981G=	GRCh38
NC_000019.9:g.6681992G= , CM000681.1:g.6681992G=	GRCh37
NC_000019.8:g.6632992G=	NCBI36
NG_009557.1:g.43671C= , LRG_27:g.43671C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2658C=
ENST00000695653.1:c.2219C=	ENSP00000512084.1:p.Ala740=
ENST00000695654.1:c.3335C=	ENSP00000512085.1:p.Ala1112=
ENST00000695689.1:c.281C=	ENSP00000512101.1:n.281C=
ENST00000695690.1:n.501C=
ENST00000695691.1:n.501C=
ENST00000245907.11:c.4310C= MANE Select	ENSP00000245907.4:p.Ala1437=
ENST00000245907.10:c.4310C=	ENSP00000245907.4:p.Ala1437=
ENST00000596548.1:c.431C=	ENSP00000469744.1:p.Ala144=
ENST00000599899.5:n.1269C=
ENST00000601008.1:c.242-4023C=	ENSP00000471384.1:n.242-4023C=
NM_000064.3:c.4310C=	NP_000055.2:p.Ala1437=
NM_000064.4:c.4310C= MANE Select	NP_000055.2:p.Ala1437=