Canonical Allele Identifier: CA2320550600

Gene: C3

Linked Data

• dbSNP Id: rs1917813939

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679829_6679857dup , CM000681.2:g.6679829_6679857dup	GRCh38
NC_000019.9:g.6679840_6679868dup , CM000681.1:g.6679840_6679868dup	GRCh37
NC_000019.8:g.6630840_6630868dup	NCBI36
NG_009557.1:g.45796_45824dup , LRG_27:g.45796_45824dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2804+302_2804+330dup
ENST00000695653.1:c.2365+302_2365+330dup	ENSP00000512084.1:n.2365+302_2365+330dup
ENST00000695654.1:c.3481+302_3481+330dup	ENSP00000512085.1:n.3481+302_3481+330dup
ENST00000695689.1:c.427+302_427+330dup	ENSP00000512101.1:n.427+302_427+330dup
ENST00000695690.1:n.1521+302_1521+330dup
ENST00000695691.1:n.1317+302_1317+330dup
ENST00000245907.11:c.4456+302_4456+330dup MANE Select	ENSP00000245907.4:n.4456+302_4456+330dup
ENST00000245907.10:c.4456+302_4456+330dup	ENSP00000245907.4:n.4456+302_4456+330dup
ENST00000599668.1:n.51+245_51+273dup
ENST00000599899.5:n.1415+302_1415+330dup
ENST00000601008.1:c.242-1898_242-1870dup	ENSP00000471384.1:n.242-1898_242-1870dup
NM_000064.3:c.4456+302_4456+330dup	NP_000055.2:n.4456+302_4456+330dup
NM_000064.4:c.4456+302_4456+330dup MANE Select	NP_000055.2:n.4456+302_4456+330dup