Canonical Allele Identifier: CA2320566087

Gene: C3

Linked Data

• dbSNP Id: rs1967870244

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710012_6710023dup , CM000681.2:g.6710012_6710023dup	GRCh38
NC_000019.9:g.6710023_6710034dup , CM000681.1:g.6710023_6710034dup	GRCh37
NC_000019.8:g.6661023_6661034dup	NCBI36
NG_009557.1:g.15634_15645dup , LRG_27:g.15634_15645dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-176_1564-165dup	ENSP00000512083.1:n.1564-176_1564-165dup
ENST00000695654.1:c.811-176_811-165dup	ENSP00000512085.1:n.811-176_811-165dup
ENST00000695655.1:c.592-140_592-129dup	ENSP00000512086.1:n.592-140_592-129dup
ENST00000695692.1:n.1051-176_1051-165dup
ENST00000245907.11:c.1687-176_1687-165dup MANE Select	ENSP00000245907.4:n.1687-176_1687-165dup
ENST00000245907.10:c.1687-176_1687-165dup	ENSP00000245907.4:n.1687-176_1687-165dup
ENST00000600763.1:n.320-176_320-165dup
NM_000064.3:c.1687-176_1687-165dup	NP_000055.2:n.1687-176_1687-165dup
NM_000064.4:c.1687-176_1687-165dup MANE Select	NP_000055.2:n.1687-176_1687-165dup