Canonical Allele Identifier: CA78941408
Gene: LINC02070 HGNC NCBI

Linked Data

dbSNP Id: rs948346339
gnomAD v2: 3-86544469-A-G
gnomAD v3: 3-86495319-A-G
gnomAD v4: 3-86495319-A-G
MyVariant Identifiers: chr3:g.86544469A>G (hg19) chr3:g.86495319A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.86495319A>G , CM000665.2:g.86495319A>G GRCh38
NC_000003.11:g.86544469A>G , CM000665.1:g.86544469A>G GRCh37
NC_000003.10:g.86627159A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245082.1:n.116-472A>G
NR_135563.1:n.116-472A>G
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