Canonical Allele Identifier: CA2198988000
Gene: LINC02351 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98332898T= , CM000677.2:g.98332898T= GRCh38
NC_000015.9:g.98876127T= , CM000677.1:g.98876127T= GRCh37
NC_000015.8:g.96693650T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_146567.1:n.191-5445A=