Canonical Allele Identifier: CA2198987976
Gene: LINC02351 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98332874G= , CM000677.2:g.98332874G= GRCh38
NC_000015.9:g.98876103G= , CM000677.1:g.98876103G= GRCh37
NC_000015.8:g.96693626G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_146567.1:n.191-5421C=