Canonical Allele Identifier: CA911527586
Gene: LINC02070 HGNC NCBI

Linked Data

dbSNP Id: rs1354687725
gnomAD v3: 3-86495368-C-T
gnomAD v4: 3-86495368-C-T
MyVariant Identifiers: chr3:g.86544518C>T (hg19) chr3:g.86495368C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.86495368C>T , CM000665.2:g.86495368C>T GRCh38
NC_000003.11:g.86544518C>T , CM000665.1:g.86544518C>T GRCh37
NC_000003.10:g.86627208C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245082.1:n.116-423C>T
NR_135563.1:n.116-423C>T
Search 100 bp 5'
Search 100 bp 3'