Canonical Allele Identifier: CA325105778
Gene: MIRLET7BHG HGNC NCBI

Linked Data

dbSNP Id: rs918982797
gnomAD v3: 22-46108299-A-G
gnomAD v4: 22-46108299-A-G
MyVariant Identifiers: chr22:g.46504179A>G (hg19) chr22:g.46108299A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46108299A>G , CM000684.2:g.46108299A>G GRCh38
NC_000022.10:g.46504179A>G , CM000684.1:g.46504179A>G GRCh37
NC_000022.9:g.44882843A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027033.2:n.373-968A>G
NR_110479.1:n.315-968A>G
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