Canonical Allele Identifier: CA2011125373
Gene: LINC02714 HGNC NCBI

Linked Data

dbSNP Id: rs1939612413

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134756956C>A , CM000673.2:g.134756956C>A GRCh38
NC_000011.9:g.134626850C>A , CM000673.1:g.134626850C>A GRCh37
NC_000011.8:g.134132060C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_147836.1:n.599-4118C>A