Canonical Allele Identifier: CA911527537
Gene: LINC02070 HGNC NCBI

Linked Data

dbSNP Id: rs1216570440
gnomAD v3: 3-86495314-T-TATA
gnomAD v4: 3-86495314-T-TATA
MyVariant Identifiers: chr3:g.86544464_86544465insATA (hg19) chr3:g.86495314_86495315insATA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.86495314_86495315insATA , CM000665.2:g.86495314_86495315insATA GRCh38
NC_000003.11:g.86544464_86544465insATA , CM000665.1:g.86544464_86544465insATA GRCh37
NC_000003.10:g.86627154_86627155insATA NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245082.1:n.116-477_116-476insATA
NR_135563.1:n.116-477_116-476insATA
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