Canonical Allele Identifier: CA717692372
Gene: LINC02351 HGNC NCBI

Linked Data

dbSNP Id: rs1428473746
gnomAD v3: 15-98332829-G-C
gnomAD v4: 15-98332829-G-C
MyVariant Identifiers: chr15:g.98876058G>C (hg19) chr15:g.98332829G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98332829G>C , CM000677.2:g.98332829G>C GRCh38
NC_000015.9:g.98876058G>C , CM000677.1:g.98876058G>C GRCh37
NC_000015.8:g.96693581G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_146567.1:n.191-5376C>G
Search 100 bp 5'
Search 100 bp 3'