Canonical Allele Identifier: CA2735579769

Gene: C3

Linked Data

• dbSNP Id: rs2145426281

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710026_6710027insA , CM000681.2:g.6710026_6710027insA	GRCh38
NC_000019.9:g.6710037_6710038insA , CM000681.1:g.6710037_6710038insA	GRCh37
NC_000019.8:g.6661037_6661038insA	NCBI36
NG_009557.1:g.15625_15626insT , LRG_27:g.15625_15626insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-185_1564-184insT	ENSP00000512083.1:n.1564-185_1564-184insT
ENST00000695654.1:c.811-185_811-184insT	ENSP00000512085.1:n.811-185_811-184insT
ENST00000695655.1:c.592-149_592-148insT	ENSP00000512086.1:n.592-149_592-148insT
ENST00000695692.1:n.1051-185_1051-184insT
ENST00000245907.11:c.1687-185_1687-184insT MANE Select	ENSP00000245907.4:n.1687-185_1687-184insT
ENST00000245907.10:c.1687-185_1687-184insT	ENSP00000245907.4:n.1687-185_1687-184insT
ENST00000600763.1:n.320-185_320-184insT
NM_000064.3:c.1687-185_1687-184insT	NP_000055.2:n.1687-185_1687-184insT
NM_000064.4:c.1687-185_1687-184insT MANE Select	NP_000055.2:n.1687-185_1687-184insT