Canonical Allele Identifier: CA1413661535
Gene: LINC00880 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.157119148_157119149delinsCA , CM000665.2:g.157119148_157119149delinsCA GRCh38
NC_000003.11:g.156836937_156836938delinsCA , CM000665.1:g.156836937_156836938delinsCA GRCh37
NC_000003.10:g.158319631_158319632delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_034007.1:n.127+3727_127+3728delinsTG