Canonical Allele Identifier: CA275722424

Gene: LINC02351

Linked Data

• dbSNP Id: rs928635676
• MyVariant Identifiers: chr15:g.98876115G>C (hg19) ; chr15:g.98332886G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98332886G>C , CM000677.2:g.98332886G>C	GRCh38
NC_000015.9:g.98876115G>C , CM000677.1:g.98876115G>C	GRCh37
NC_000015.8:g.96693638G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_146567.1:n.191-5433C>G