Canonical Allele Identifier: CA544492174
Gene: LINC02070 HGNC NCBI

Linked Data

dbSNP Id: rs1377929523
gnomAD v2: 3-86544463-G-T
gnomAD v3: 3-86495313-G-T
gnomAD v4: 3-86495313-G-T
MyVariant Identifiers: chr3:g.86544463G>T (hg19) chr3:g.86495313G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.86495313G>T , CM000665.2:g.86495313G>T GRCh38
NC_000003.11:g.86544463G>T , CM000665.1:g.86544463G>T GRCh37
NC_000003.10:g.86627153G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245082.1:n.116-478G>T
NR_135563.1:n.116-478G>T
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