Canonical Allele Identifier: CA2198987993
Gene: LINC02351 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98332891A= , CM000677.2:g.98332891A= GRCh38
NC_000015.9:g.98876120A= , CM000677.1:g.98876120A= GRCh37
NC_000015.8:g.96693643A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_146567.1:n.191-5438T=