Canonical Allele Identifier: CA2320551539

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6681969C= , CM000681.2:g.6681969C=	GRCh38
NC_000019.9:g.6681980C= , CM000681.1:g.6681980C=	GRCh37
NC_000019.8:g.6632980C=	NCBI36
NG_009557.1:g.43683G= , LRG_27:g.43683G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2670G=
ENST00000695653.1:c.2231G=	ENSP00000512084.1:p.Arg744=
ENST00000695654.1:c.3347G=	ENSP00000512085.1:p.Arg1116=
ENST00000695689.1:c.293G=	ENSP00000512101.1:n.293G=
ENST00000695690.1:n.513G=
ENST00000695691.1:n.513G=
ENST00000245907.11:c.4322G= MANE Select	ENSP00000245907.4:p.Arg1441=
ENST00000245907.10:c.4322G=	ENSP00000245907.4:p.Arg1441=
ENST00000596548.1:c.443G=	ENSP00000469744.1:p.Arg148=
ENST00000599899.5:n.1281G=
ENST00000601008.1:c.242-4011G=	ENSP00000471384.1:n.242-4011G=
NM_000064.3:c.4322G=	NP_000055.2:p.Arg1441=
NM_000064.4:c.4322G= MANE Select	NP_000055.2:p.Arg1441=