Canonical Allele Identifier: CA603029873
Gene: LINC02714 HGNC NCBI

Linked Data

dbSNP Id: rs1264363037
gnomAD v2: 11-134626785-T-A
gnomAD v3: 11-134756891-T-A
gnomAD v4: 11-134756891-T-A
MyVariant Identifiers: chr11:g.134626785T>A (hg19) chr11:g.134756891T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134756891T>A , CM000673.2:g.134756891T>A GRCh38
NC_000011.9:g.134626785T>A , CM000673.1:g.134626785T>A GRCh37
NC_000011.8:g.134131995T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_147836.1:n.599-4183T>A
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