Canonical Allele Identifier: CA325106999
Gene: MIRLET7BHG HGNC NCBI

Linked Data

dbSNP Id: rs576319282
gnomAD v2: 22-46507484-A-T
gnomAD v3: 22-46111604-A-T
gnomAD v4: 22-46111604-A-T
MyVariant Identifiers: chr22:g.46507484A>T (hg19) chr22:g.46111604A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46111604A>T , CM000684.2:g.46111604A>T GRCh38
NC_000022.10:g.46507484A>T , CM000684.1:g.46507484A>T GRCh37
NC_000022.9:g.44886148A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027033.2:n.2393A>T
NR_110479.1:n.2242A>T
Search 100 bp 5'
Search 100 bp 3'