Canonical Allele Identifier: CA325105733
Gene: MIRLET7BHG HGNC NCBI

Linked Data

dbSNP Id: rs576598741
gnomAD v2: 22-46504086-G-A
gnomAD v3: 22-46108206-G-A
gnomAD v4: 22-46108206-G-A
MyVariant Identifiers: chr22:g.46504086G>A (hg19) chr22:g.46108206G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46108206G>A , CM000684.2:g.46108206G>A GRCh38
NC_000022.10:g.46504086G>A , CM000684.1:g.46504086G>A GRCh37
NC_000022.9:g.44882750G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027033.2:n.373-1061G>A
NR_110479.1:n.315-1061G>A
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