Canonical Allele Identifier: CA1050453423
Gene: LINC02070 HGNC NCBI

Linked Data

dbSNP Id: rs1704106001
gnomAD v3: 3-86495238-T-G
gnomAD v4: 3-86495238-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.86495238T>G , CM000665.2:g.86495238T>G GRCh38
NC_000003.11:g.86544388T>G , CM000665.1:g.86544388T>G GRCh37
NC_000003.10:g.86627078T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245082.1:n.116-553T>G
NR_135563.1:n.116-553T>G
Search 100 bp 5'
Search 100 bp 3'