Canonical Allele Identifier: CA603029870
Gene: LINC02714 HGNC NCBI

Linked Data

dbSNP Id: rs1312320136
gnomAD v2: 11-134626712-G-A
MyVariant Identifiers: chr11:g.134626712G>A (hg19) chr11:g.134756818G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134756818G>A , CM000673.2:g.134756818G>A GRCh38
NC_000011.9:g.134626712G>A , CM000673.1:g.134626712G>A GRCh37
NC_000011.8:g.134131922G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_147836.1:n.599-4256G>A
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