Canonical Allele Identifier: CA325105881
Gene: MIRLET7BHG HGNC NCBI

Linked Data

dbSNP Id: rs576194604
gnomAD v3: 22-46108561-G-C
gnomAD v4: 22-46108561-G-C
MyVariant Identifiers: chr22:g.46504441G>C (hg19) chr22:g.46108561G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46108561G>C , CM000684.2:g.46108561G>C GRCh38
NC_000022.10:g.46504441G>C , CM000684.1:g.46504441G>C GRCh37
NC_000022.9:g.44883105G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027033.2:n.373-706G>C
NR_110479.1:n.315-706G>C
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