Canonical Allele Identifier: CA2320551558

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682020C= , CM000681.2:g.6682020C=	GRCh38
NC_000019.9:g.6682031C= , CM000681.1:g.6682031C=	GRCh37
NC_000019.8:g.6633031C=	NCBI36
NG_009557.1:g.43632G= , LRG_27:g.43632G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2619G=
ENST00000695653.1:c.2180G=	ENSP00000512084.1:p.Gly727=
ENST00000695654.1:c.3296G=	ENSP00000512085.1:p.Gly1099=
ENST00000695689.1:c.242G=	ENSP00000512101.1:n.242G=
ENST00000695690.1:n.462G=
ENST00000695691.1:n.462G=
ENST00000245907.11:c.4271G= MANE Select	ENSP00000245907.4:p.Gly1424=
ENST00000245907.10:c.4271G=	ENSP00000245907.4:p.Gly1424=
ENST00000596548.1:c.392G=	ENSP00000469744.1:p.Gly131=
ENST00000599899.5:n.1230G=
ENST00000601008.1:c.242-4062G=	ENSP00000471384.1:n.242-4062G=
NM_000064.3:c.4271G=	NP_000055.2:p.Gly1424=
NM_000064.4:c.4271G= MANE Select	NP_000055.2:p.Gly1424=