Canonical Allele Identifier: CA2320550635

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679894G= , CM000681.2:g.6679894G=	GRCh38
NC_000019.9:g.6679905G= , CM000681.1:g.6679905G=	GRCh37
NC_000019.8:g.6630905G=	NCBI36
NG_009557.1:g.45758C= , LRG_27:g.45758C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2804+264C=
ENST00000695653.1:c.2365+264C=	ENSP00000512084.1:n.2365+264C=
ENST00000695654.1:c.3481+264C=	ENSP00000512085.1:n.3481+264C=
ENST00000695689.1:c.427+264C=	ENSP00000512101.1:n.427+264C=
ENST00000695690.1:n.1521+264C=
ENST00000695691.1:n.1317+264C=
ENST00000245907.11:c.4456+264C= MANE Select	ENSP00000245907.4:n.4456+264C=
ENST00000245907.10:c.4456+264C=	ENSP00000245907.4:n.4456+264C=
ENST00000599668.1:n.51+207C=
ENST00000599899.5:n.1415+264C=
ENST00000601008.1:c.242-1936C=	ENSP00000471384.1:n.242-1936C=
NM_000064.3:c.4456+264C=	NP_000055.2:n.4456+264C=
NM_000064.4:c.4456+264C= MANE Select	NP_000055.2:n.4456+264C=