Canonical Allele Identifier: CA673874915
Gene: LINC02714 HGNC NCBI

Linked Data

dbSNP Id: rs1254394671

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134756939G>T , CM000673.2:g.134756939G>T GRCh38
NC_000011.9:g.134626833G>T , CM000673.1:g.134626833G>T GRCh37
NC_000011.8:g.134132043G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_147836.1:n.599-4135G>T