Canonical Allele Identifier: CA2320551533

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6681950G= , CM000681.2:g.6681950G=	GRCh38
NC_000019.9:g.6681961G= , CM000681.1:g.6681961G=	GRCh37
NC_000019.8:g.6632961G=	NCBI36
NG_009557.1:g.43702C= , LRG_27:g.43702C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2689C=
ENST00000695653.1:c.2250C=	ENSP00000512084.1:p.Tyr750=
ENST00000695654.1:c.3366C=	ENSP00000512085.1:p.Tyr1122=
ENST00000695689.1:c.312C=	ENSP00000512101.1:n.312C=
ENST00000695690.1:n.532C=
ENST00000695691.1:n.532C=
ENST00000245907.11:c.4341C= MANE Select	ENSP00000245907.4:p.Tyr1447=
ENST00000245907.10:c.4341C=	ENSP00000245907.4:p.Tyr1447=
ENST00000596548.1:c.462C=	ENSP00000469744.1:p.Tyr154=
ENST00000599899.5:n.1300C=
ENST00000601008.1:c.242-3992C=	ENSP00000471384.1:n.242-3992C=
NM_000064.3:c.4341C=	NP_000055.2:p.Tyr1447=
NM_000064.4:c.4341C= MANE Select	NP_000055.2:p.Tyr1447=