Canonical Allele Identifier: CA943861429
Gene: LINC02714 HGNC NCBI

Linked Data

dbSNP Id: rs1939611702

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134756878A>T , CM000673.2:g.134756878A>T GRCh38
NC_000011.9:g.134626772A>T , CM000673.1:g.134626772A>T GRCh37
NC_000011.8:g.134131982A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_147836.1:n.599-4196A>T