Canonical Allele Identifier: CA1026264619
Gene: MIRLET7BHG HGNC NCBI

Linked Data

dbSNP Id: rs1922842833
gnomAD v3: 22-46108360-TG-T
gnomAD v4: 22-46108360-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46108363del , CM000684.2:g.46108363del GRCh38
NC_000022.10:g.46504243del , CM000684.1:g.46504243del GRCh37
NC_000022.9:g.44882907del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027033.2:n.373-904del
NR_110479.1:n.315-904del
Search 100 bp 5'
Search 100 bp 3'