Canonical Allele Identifier: CA1055324273
Gene: LINC00880 HGNC NCBI

Linked Data

dbSNP Id: rs1979485

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.157119176C>A , CM000665.2:g.157119176C>A GRCh38
NC_000003.11:g.156836965C>A , CM000665.1:g.156836965C>A GRCh37
NC_000003.10:g.158319659C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_034007.1:n.127+3700G>T