Canonical Allele Identifier: CA673874826
Gene: LINC02714 HGNC NCBI

Linked Data

dbSNP Id: rs1390576954

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134756797A>G , CM000673.2:g.134756797A>G GRCh38
NC_000011.9:g.134626691A>G , CM000673.1:g.134626691A>G GRCh37
NC_000011.8:g.134131901A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_147836.1:n.599-4277A>G