Canonical Allele Identifier: CA639630638
Gene: MIRLET7BHG HGNC NCBI

Linked Data

dbSNP Id: rs1476519264
gnomAD v2: 22-46504092-G-C
gnomAD v3: 22-46108212-G-C
gnomAD v4: 22-46108212-G-C
MyVariant Identifiers: chr22:g.46504092G>C (hg19) chr22:g.46108212G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46108212G>C , CM000684.2:g.46108212G>C GRCh38
NC_000022.10:g.46504092G>C , CM000684.1:g.46504092G>C GRCh37
NC_000022.9:g.44882756G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027033.2:n.373-1055G>C
NR_110479.1:n.315-1055G>C
Search 100 bp 5'
Search 100 bp 3'