Canonical Allele Identifier: CA2011125217
Gene: LINC02714 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134756796T= , CM000673.2:g.134756796T= GRCh38
NC_000011.9:g.134626690T= , CM000673.1:g.134626690T= GRCh37
NC_000011.8:g.134131900T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_147836.1:n.599-4278T=