Canonical Allele Identifier: CA2320566082
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1967870082

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6710025_6710026insAGGGAGAGAGAGGGAGAGAGGGCGGGAGAGAGAGGGAGAGAGGG , CM000681.2:g.6710025_6710026insAGGGAGAGAGAGGGAGAGAGGGCGGGAGAGAGAGGGAGAGAGGG GRCh38
NC_000019.9:g.6710036_6710037insAGGGAGAGAGAGGGAGAGAGGGCGGGAGAGAGAGGGAGAGAGGG , CM000681.1:g.6710036_6710037insAGGGAGAGAGAGGGAGAGAGGGCGGGAGAGAGAGGGAGAGAGGG GRCh37
NC_000019.8:g.6661036_6661037insAGGGAGAGAGAGGGAGAGAGGGCGGGAGAGAGAGGGAGAGAGGG NCBI36
NG_009557.1:g.15647_15648insGCCCTCTCTCCCTCTCTCTCCCTCCCTCTCTCCCTCTCTCTCCC , LRG_27:g.15647_15648insGCCCTCTCTCCCTCTCTCTCCCTCCCTCTCTCCCTCTCTCTCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1564-163_1564-162insGCCCTCTCTCCCTCTCTCTCCCTCCCTCTCTCCCTCTCTCTCCC ENSP00000512083.1:n.1564-163_1564-162insGCCCTCTCTCCCTCTCTCTCC...
ENST00000695654.1:c.811-163_811-162insGCCCTCTCTCCCTCTCTCTCCCTCCCTCTCTCCCTCTCTCTCCC ENSP00000512085.1:n.811-163_811-162insGCCCTCTCTCCCTCTCTCTCCCT...
ENST00000695655.1:c.592-127_592-126insGCCCTCTCTCCCTCTCTCTCCCTCCCTCTCTCCCTCTCTCTCCC ENSP00000512086.1:n.592-127_592-126insGCCCTCTCTCCCTCTCTCTCCCT...
ENST00000695692.1:n.1051-163_1051-162insGCCCTCTCTCCCTCTCTCTCCCTCCCTCTCTCCCTCTCTCTCCC
ENST00000245907.11:c.1687-163_1687-162insGCCCTCTCTCCCTCTCTCTCCCTCCCTCTCTCCCTCTCTCTCCC MANE Select ENSP00000245907.4:n.1687-163_1687-162insGCCCTCTCTCCCTCTCTCTCC...
ENST00000245907.10:c.1687-163_1687-162insGCCCTCTCTCCCTCTCTCTCCCTCCCTCTCTCCCTCTCTCTCCC ENSP00000245907.4:n.1687-163_1687-162insGCCCTCTCTCCCTCTCTCTCC...
ENST00000600763.1:n.320-163_320-162insGCCCTCTCTCCCTCTCTCTCCCTCCCTCTCTCCCTCTCTCTCCC
NM_000064.3:c.1687-163_1687-162insGCCCTCTCTCCCTCTCTCTCCCTCCCTCTCTCCCTCTCTCTCCC NP_000055.2:n.1687-163_1687-162insGCCCTCTCTCCCTCTCTCTCCCTCCCT...
NM_000064.4:c.1687-163_1687-162insGCCCTCTCTCCCTCTCTCTCCCTCCCTCTCTCCCTCTCTCTCCC MANE Select NP_000055.2:n.1687-163_1687-162insGCCCTCTCTCCCTCTCTCTCCCTCCCT...