Canonical Allele Identifier: CA990758931
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs576343975
gnomAD v3: 18-58450095-C-A
gnomAD v4: 18-58450095-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450095C>A , CM000680.2:g.58450095C>A GRCh38
NC_000018.9:g.56117327C>A , CM000680.1:g.56117327C>A GRCh37
NC_000018.8:g.54268307C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1334C>A
NR_170243.1:n.308-396C>A
NR_170244.1:n.307+555C>A
NR_170245.1:n.307+555C>A
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