Canonical Allele Identifier: CA275722425
Gene: LINC02351 HGNC NCBI

Linked Data

dbSNP Id: rs377683487
MyVariant Identifiers: chr15:g.98876124C>A (hg19) chr15:g.98332895C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98332895C>A , CM000677.2:g.98332895C>A GRCh38
NC_000015.9:g.98876124C>A , CM000677.1:g.98876124C>A GRCh37
NC_000015.8:g.96693647C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_146567.1:n.191-5442G>T
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