Canonical Allele Identifier: CA325105738
Gene: MIRLET7BHG HGNC NCBI

Linked Data

dbSNP Id: rs945689787
gnomAD v3: 22-46108228-T-C
gnomAD v4: 22-46108228-T-C
MyVariant Identifiers: chr22:g.46504108T>C (hg19) chr22:g.46108228T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46108228T>C , CM000684.2:g.46108228T>C GRCh38
NC_000022.10:g.46504108T>C , CM000684.1:g.46504108T>C GRCh37
NC_000022.9:g.44882772T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027033.2:n.373-1039T>C
NR_110479.1:n.315-1039T>C
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