Canonical Allele Identifier: CA325105812
Gene: MIRLET7BHG HGNC NCBI

Linked Data

dbSNP Id: rs1039443887
gnomAD v3: 22-46108407-C-T
gnomAD v4: 22-46108407-C-T
MyVariant Identifiers: chr22:g.46504287C>T (hg19) chr22:g.46108407C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46108407C>T , CM000684.2:g.46108407C>T GRCh38
NC_000022.10:g.46504287C>T , CM000684.1:g.46504287C>T GRCh37
NC_000022.9:g.44882951C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027033.2:n.373-860C>T
NR_110479.1:n.315-860C>T
Search 100 bp 5'
Search 100 bp 3'