Canonical Allele Identifier: CA2735579675
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs2145426232

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6710025_6710026insAGGGAGAGAGAGTGAGAGAGGG , CM000681.2:g.6710025_6710026insAGGGAGAGAGAGTGAGAGAGGG GRCh38
NC_000019.9:g.6710036_6710037insAGGGAGAGAGAGTGAGAGAGGG , CM000681.1:g.6710036_6710037insAGGGAGAGAGAGTGAGAGAGGG GRCh37
NC_000019.8:g.6661036_6661037insAGGGAGAGAGAGTGAGAGAGGG NCBI36
NG_009557.1:g.15635_15636insACTCTCTCTCCCTCCCTCTCTC , LRG_27:g.15635_15636insACTCTCTCTCCCTCCCTCTCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1564-175_1564-174insACTCTCTCTCCCTCCCTCTCTC ENSP00000512083.1:n.1564-175_1564-174insACTCTCTCTCCCTCCCTCTCT...
ENST00000695654.1:c.811-175_811-174insACTCTCTCTCCCTCCCTCTCTC ENSP00000512085.1:n.811-175_811-174insACTCTCTCTCCCTCCCTCTCTC
ENST00000695655.1:c.592-139_592-138insACTCTCTCTCCCTCCCTCTCTC ENSP00000512086.1:n.592-139_592-138insACTCTCTCTCCCTCCCTCTCTC
ENST00000695692.1:n.1051-175_1051-174insACTCTCTCTCCCTCCCTCTCTC
ENST00000245907.11:c.1687-175_1687-174insACTCTCTCTCCCTCCCTCTCTC MANE Select ENSP00000245907.4:n.1687-175_1687-174insACTCTCTCTCCCTCCCTCTCT...
ENST00000245907.10:c.1687-175_1687-174insACTCTCTCTCCCTCCCTCTCTC ENSP00000245907.4:n.1687-175_1687-174insACTCTCTCTCCCTCCCTCTCT...
ENST00000600763.1:n.320-175_320-174insACTCTCTCTCCCTCCCTCTCTC
NM_000064.3:c.1687-175_1687-174insACTCTCTCTCCCTCCCTCTCTC NP_000055.2:n.1687-175_1687-174insACTCTCTCTCCCTCCCTCTCTC
NM_000064.4:c.1687-175_1687-174insACTCTCTCTCCCTCCCTCTCTC MANE Select NP_000055.2:n.1687-175_1687-174insACTCTCTCTCCCTCCCTCTCTC