Canonical Allele Identifier: CA78941383
Gene: LINC02070 HGNC NCBI

Linked Data

dbSNP Id: rs188655146
gnomAD v2: 3-86544386-T-G
gnomAD v3: 3-86495236-T-G
gnomAD v4: 3-86495236-T-G
MyVariant Identifiers: chr3:g.86544386T>G (hg19) chr3:g.86495236T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.86495236T>G , CM000665.2:g.86495236T>G GRCh38
NC_000003.11:g.86544386T>G , CM000665.1:g.86544386T>G GRCh37
NC_000003.10:g.86627076T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245082.1:n.116-555T>G
NR_135563.1:n.116-555T>G
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