Canonical Allele Identifier: CA603029879
Gene: LINC02714 HGNC NCBI

Linked Data

dbSNP Id: rs1433883676

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134756930C>T , CM000673.2:g.134756930C>T GRCh38
NC_000011.9:g.134626824C>T , CM000673.1:g.134626824C>T GRCh37
NC_000011.8:g.134132034C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_147836.1:n.599-4144C>T