Canonical Allele Identifier: CA2011125215
Gene: LINC02714 HGNC NCBI

Linked Data

dbSNP Id: rs1591754439

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134756794A>C , CM000673.2:g.134756794A>C GRCh38
NC_000011.9:g.134626688A>C , CM000673.1:g.134626688A>C GRCh37
NC_000011.8:g.134131898A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_147836.1:n.599-4280A>C