Canonical Allele Identifier: CA325105803
Gene: MIRLET7BHG HGNC NCBI

Linked Data

dbSNP Id: rs537811639
gnomAD v3: 22-46108387-G-A
gnomAD v4: 22-46108387-G-A
MyVariant Identifiers: chr22:g.46504267G>A (hg19) chr22:g.46108387G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46108387G>A , CM000684.2:g.46108387G>A GRCh38
NC_000022.10:g.46504267G>A , CM000684.1:g.46504267G>A GRCh37
NC_000022.9:g.44882931G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027033.2:n.373-880G>A
NR_110479.1:n.315-880G>A
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