Canonical Allele Identifier: CA2011125222
Gene: LINC02714 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134756797A= , CM000673.2:g.134756797A= GRCh38
NC_000011.9:g.134626691A= , CM000673.1:g.134626691A= GRCh37
NC_000011.8:g.134131901A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_147836.1:n.599-4277A=