Canonical Allele Identifier: CA2320551648

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682222C= , CM000681.2:g.6682222C=	GRCh38
NC_000019.9:g.6682233C= , CM000681.1:g.6682233C=	GRCh37
NC_000019.8:g.6633233C=	NCBI36
NG_009557.1:g.43430G= , LRG_27:g.43430G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2528G=
ENST00000695653.1:c.2089G=	ENSP00000512084.1:p.Gly697=
ENST00000695654.1:c.3205G=	ENSP00000512085.1:p.Gly1069=
ENST00000695689.1:c.151G=	ENSP00000512101.1:n.151G=
ENST00000695690.1:n.371G=
ENST00000695691.1:n.371G=
ENST00000245907.11:c.4180G= MANE Select	ENSP00000245907.4:p.Gly1394=
ENST00000245907.10:c.4180G=	ENSP00000245907.4:p.Gly1394=
ENST00000596548.1:c.301G=	ENSP00000469744.1:p.Gly101=
ENST00000599899.5:n.1139G=
ENST00000601008.1:c.242-4264G=	ENSP00000471384.1:n.242-4264G=
NM_000064.3:c.4180G=	NP_000055.2:p.Gly1394=
NM_000064.4:c.4180G= MANE Select	NP_000055.2:p.Gly1394=