Canonical Allele Identifier: CA2735579825

Gene: C3

Linked Data

• dbSNP Id: rs2145426315

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710037_6710038insGGAGAGAGGGAGGGAGAGTGAG , CM000681.2:g.6710037_6710038insGGAGAGAGGGAGGGAGAGTGAG	GRCh38
NC_000019.9:g.6710048_6710049insGGAGAGAGGGAGGGAGAGTGAG , CM000681.1:g.6710048_6710049insGGAGAGAGGGAGGGAGAGTGAG	GRCh37
NC_000019.8:g.6661048_6661049insGGAGAGAGGGAGGGAGAGTGAG	NCBI36
NG_009557.1:g.15617_15618insACTCTCCCTCCCTCTCTCCCTC , LRG_27:g.15617_15618insACTCTCCCTCCCTCTCTCCCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-193_1564-192insACTCTCCCTCCCTCTCTCCCTC	ENSP00000512083.1:n.1564-193_1564-192insACTCTCCCTCCCTCTCTCCCT...
ENST00000695654.1:c.811-193_811-192insACTCTCCCTCCCTCTCTCCCTC	ENSP00000512085.1:n.811-193_811-192insACTCTCCCTCCCTCTCTCCCTC
ENST00000695655.1:c.592-157_592-156insACTCTCCCTCCCTCTCTCCCTC	ENSP00000512086.1:n.592-157_592-156insACTCTCCCTCCCTCTCTCCCTC
ENST00000695692.1:n.1051-193_1051-192insACTCTCCCTCCCTCTCTCCCTC
ENST00000245907.11:c.1687-193_1687-192insACTCTCCCTCCCTCTCTCCCTC MANE Select	ENSP00000245907.4:n.1687-193_1687-192insACTCTCCCTCCCTCTCTCCCT...
ENST00000245907.10:c.1687-193_1687-192insACTCTCCCTCCCTCTCTCCCTC	ENSP00000245907.4:n.1687-193_1687-192insACTCTCCCTCCCTCTCTCCCT...
ENST00000600763.1:n.320-193_320-192insACTCTCCCTCCCTCTCTCCCTC
NM_000064.3:c.1687-193_1687-192insACTCTCCCTCCCTCTCTCCCTC	NP_000055.2:n.1687-193_1687-192insACTCTCCCTCCCTCTCTCCCTC
NM_000064.4:c.1687-193_1687-192insACTCTCCCTCCCTCTCTCCCTC MANE Select	NP_000055.2:n.1687-193_1687-192insACTCTCCCTCCCTCTCTCCCTC