Canonical Allele Identifier: CA753659561
Gene: MIRLET7BHG HGNC NCBI

Linked Data

dbSNP Id: rs1162634801
gnomAD v3: 22-46108478-C-G
gnomAD v4: 22-46108478-C-G
MyVariant Identifiers: chr22:g.46504358C>G (hg19) chr22:g.46108478C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46108478C>G , CM000684.2:g.46108478C>G GRCh38
NC_000022.10:g.46504358C>G , CM000684.1:g.46504358C>G GRCh37
NC_000022.9:g.44883022C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027033.2:n.373-789C>G
NR_110479.1:n.315-789C>G
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