Canonical Allele Identifier: CA673874882
Gene: LINC02714 HGNC NCBI

Linked Data

dbSNP Id: rs1370933503

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134756896G>A , CM000673.2:g.134756896G>A GRCh38
NC_000011.9:g.134626790G>A , CM000673.1:g.134626790G>A GRCh37
NC_000011.8:g.134132000G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_147836.1:n.599-4178G>A