Canonical Allele Identifier: CA639630640
Gene: MIRLET7BHG HGNC NCBI

Linked Data

dbSNP Id: rs1201026662
gnomAD v2: 22-46504107-A-T
gnomAD v3: 22-46108227-A-T
gnomAD v4: 22-46108227-A-T
MyVariant Identifiers: chr22:g.46504107A>T (hg19) chr22:g.46108227A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46108227A>T , CM000684.2:g.46108227A>T GRCh38
NC_000022.10:g.46504107A>T , CM000684.1:g.46504107A>T GRCh37
NC_000022.9:g.44882771A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027033.2:n.373-1040A>T
NR_110479.1:n.315-1040A>T
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