Canonical Allele Identifier: CA1413661413
Gene: LINC00880 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.157119048_157119049delinsGT , CM000665.2:g.157119048_157119049delinsGT GRCh38
NC_000003.11:g.156836837_156836838delinsGT , CM000665.1:g.156836837_156836838delinsGT GRCh37
NC_000003.10:g.158319531_158319532delinsGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_034007.1:n.127+3827_127+3828delinsAC