Canonical Allele Identifier: CA2011125410
Gene: LINC02714 HGNC NCBI

Linked Data

dbSNP Id: rs1939612732

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134756981A>T , CM000673.2:g.134756981A>T GRCh38
NC_000011.9:g.134626875A>T , CM000673.1:g.134626875A>T GRCh37
NC_000011.8:g.134132085A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_147836.1:n.599-4093A>T