Canonical Allele Identifier: CA14092813
Gene: LINC02351 HGNC NCBI

Linked Data

dbSNP Id: rs970843

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98332800G>C , CM000677.2:g.98332800G>C GRCh38
NC_000015.9:g.98876029G>C , CM000677.1:g.98876029G>C GRCh37
NC_000015.8:g.96693552G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_146567.1:n.191-5347C>G