Canonical Allele Identifier: CA325105854
Gene: MIRLET7BHG HGNC NCBI

Linked Data

dbSNP Id: rs986712488
gnomAD v2: 22-46504389-C-A
gnomAD v3: 22-46108509-C-A
gnomAD v4: 22-46108509-C-A
MyVariant Identifiers: chr22:g.46504389C>A (hg19) chr22:g.46108509C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46108509C>A , CM000684.2:g.46108509C>A GRCh38
NC_000022.10:g.46504389C>A , CM000684.1:g.46504389C>A GRCh37
NC_000022.9:g.44883053C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027033.2:n.373-758C>A
NR_110479.1:n.315-758C>A
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