Canonical Allele Identifier: CA300903760
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs1053653022
gnomAD v3: 18-58450086-T-C
gnomAD v4: 18-58450086-T-C
MyVariant Identifiers: chr18:g.56117318T>C (hg19) chr18:g.58450086T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450086T>C , CM000680.2:g.58450086T>C GRCh38
NC_000018.9:g.56117318T>C , CM000680.1:g.56117318T>C GRCh37
NC_000018.8:g.54268298T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1325T>C
NR_170243.1:n.308-405T>C
NR_170244.1:n.307+546T>C
NR_170245.1:n.307+546T>C
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