Canonical Allele Identifier: CA656446943
Gene: LINC02351 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98332823C>A , CM000677.2:g.98332823C>A GRCh38
NC_000015.9:g.98876052C>A , CM000677.1:g.98876052C>A GRCh37
NC_000015.8:g.96693575C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_146567.1:n.191-5370G>T