Canonical Allele Identifier: CA78941413
Gene: LINC02070 HGNC NCBI

Linked Data

dbSNP Id: rs186163345
gnomAD v2: 3-86544548-G-T
gnomAD v3: 3-86495398-G-T
gnomAD v4: 3-86495398-G-T
MyVariant Identifiers: chr3:g.86544548G>T (hg19) chr3:g.86495398G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.86495398G>T , CM000665.2:g.86495398G>T GRCh38
NC_000003.11:g.86544548G>T , CM000665.1:g.86544548G>T GRCh37
NC_000003.10:g.86627238G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245082.1:n.116-393G>T
NR_135563.1:n.116-393G>T
Search 100 bp 5'
Search 100 bp 3'