Canonical Allele Identifier: CA1413661580
Gene: LINC00880 HGNC NCBI

Linked Data

dbSNP Id: rs1737283420

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.157119207_157119208insTAATGGCTGAAAGATGCATGATGAAAGGTTGTATA , CM000665.2:g.157119207_157119208insTAATGGCTGAAAGATGCATGATGAAAGGTTGTATA GRCh38
NC_000003.11:g.156836996_156836997insTAATGGCTGAAAGATGCATGATGAAAGGTTGTATA , CM000665.1:g.156836996_156836997insTAATGGCTGAAAGATGCATGATGAAAGGTTGTATA GRCh37
NC_000003.10:g.158319690_158319691insTAATGGCTGAAAGATGCATGATGAAAGGTTGTATA NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_034007.1:n.127+3669_127+3670insATACAACCTTTCATCATGCATCTTTCAGCCATTAT