Canonical Allele Identifier: CA943861490
Gene: LINC02714 HGNC NCBI

Linked Data

dbSNP Id: rs750366111

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134757066T>A , CM000673.2:g.134757066T>A GRCh38
NC_000011.9:g.134626960T>A , CM000673.1:g.134626960T>A GRCh37
NC_000011.8:g.134132170T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_147836.1:n.599-4008T>A