Canonical Allele Identifier: CA1381162966
Gene: LINC02070 HGNC NCBI

Linked Data

dbSNP Id: rs1704111556
gnomAD v3: 3-86495356-C-G
gnomAD v4: 3-86495356-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.86495356C>G , CM000665.2:g.86495356C>G GRCh38
NC_000003.11:g.86544506C>G , CM000665.1:g.86544506C>G GRCh37
NC_000003.10:g.86627196C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245082.1:n.116-435C>G
NR_135563.1:n.116-435C>G
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