Canonical Allele Identifier: CA2320551545

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6681977G= , CM000681.2:g.6681977G=	GRCh38
NC_000019.9:g.6681988G= , CM000681.1:g.6681988G=	GRCh37
NC_000019.8:g.6632988G=	NCBI36
NG_009557.1:g.43675C= , LRG_27:g.43675C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2662C=
ENST00000695653.1:c.2223C=	ENSP00000512084.1:p.Phe741=
ENST00000695654.1:c.3339C=	ENSP00000512085.1:p.Phe1113=
ENST00000695689.1:c.285C=	ENSP00000512101.1:n.285C=
ENST00000695690.1:n.505C=
ENST00000695691.1:n.505C=
ENST00000245907.11:c.4314C= MANE Select	ENSP00000245907.4:p.Phe1438=
ENST00000245907.10:c.4314C=	ENSP00000245907.4:p.Phe1438=
ENST00000596548.1:c.435C=	ENSP00000469744.1:p.Phe145=
ENST00000599899.5:n.1273C=
ENST00000601008.1:c.242-4019C=	ENSP00000471384.1:n.242-4019C=
NM_000064.3:c.4314C=	NP_000055.2:p.Phe1438=
NM_000064.4:c.4314C= MANE Select	NP_000055.2:p.Phe1438=