Canonical Allele Identifier: CA325105789
Gene: MIRLET7BHG HGNC NCBI

Linked Data

dbSNP Id: rs752245143
gnomAD v3: 22-46108347-C-T
gnomAD v4: 22-46108347-C-T
MyVariant Identifiers: chr22:g.46504227C>T (hg19) chr22:g.46108347C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46108347C>T , CM000684.2:g.46108347C>T GRCh38
NC_000022.10:g.46504227C>T , CM000684.1:g.46504227C>T GRCh37
NC_000022.9:g.44882891C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027033.2:n.373-920C>T
NR_110479.1:n.315-920C>T
Search 100 bp 5'
Search 100 bp 3'