Canonical Allele Identifier: CA2011125346
Gene: LINC02714 HGNC NCBI

Linked Data

dbSNP Id: rs1369321284

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134756936G>C , CM000673.2:g.134756936G>C GRCh38
NC_000011.9:g.134626830G>C , CM000673.1:g.134626830G>C GRCh37
NC_000011.8:g.134132040G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_147836.1:n.599-4138G>C