Canonical Allele Identifier: CA1468958308
Gene: LINC02562 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.75105711A= , CM000666.2:g.75105711A= GRCh38
NC_000004.11:g.76030921A= , CM000666.1:g.76030921A= GRCh37
NC_000004.10:g.76249945A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938888.1:n.236-4296T=
XR_938889.1:n.135-4296T=