Canonical Allele Identifier: CA1413661399
Gene: LINC00880 HGNC NCBI

Linked Data

dbSNP Id: rs1737280626

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.157119032dup , CM000665.2:g.157119032dup GRCh38
NC_000003.11:g.156836821dup , CM000665.1:g.156836821dup GRCh37
NC_000003.10:g.158319515dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_034007.1:n.127+3848dup