Canonical Allele Identifier: CA1248392537
Gene: LINC02580 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43098432A= , CM000664.2:g.43098432A= GRCh38
NC_000002.11:g.43325570A= , CM000664.1:g.43325570A= GRCh37
NC_000002.10:g.43179074A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_109976.1:n.412-392T=
XR_940021.1:n.362-392T=
XR_940022.1:n.198-392T=
XR_940023.1:n.593-392T=
XR_940024.1:n.860-392T=
XR_940025.1:n.196-392T=
XR_940026.1:n.488-392T=
XR_940027.1:n.920-392T=
XR_940028.1:n.922-392T=
NR_151714.1:n.412-392T=