Canonical Allele Identifier: CA717692365
Gene: LINC02351 HGNC NCBI

Linked Data

dbSNP Id: rs1359462410
MyVariant Identifiers: chr15:g.98876037C>T (hg19) chr15:g.98332808C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98332808C>T , CM000677.2:g.98332808C>T GRCh38
NC_000015.9:g.98876037C>T , CM000677.1:g.98876037C>T GRCh37
NC_000015.8:g.96693560C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_146567.1:n.191-5355G>A
Search 100 bp 5'
Search 100 bp 3'