Canonical Allele Identifier: CA2011125298
Gene: LINC02714 HGNC NCBI

Linked Data

dbSNP Id: rs1939611745

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134756882G>C , CM000673.2:g.134756882G>C GRCh38
NC_000011.9:g.134626776G>C , CM000673.1:g.134626776G>C GRCh37
NC_000011.8:g.134131986G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_147836.1:n.599-4192G>C