Canonical Allele Identifier: CA504025003
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs1207683441
gnomAD v3: 18-58449618-G-A
gnomAD v4: 18-58449618-G-A
MyVariant Identifiers: chr18:g.56116850G>A (hg19) chr18:g.58449618G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449618G>A , CM000680.2:g.58449618G>A GRCh38
NC_000018.9:g.56116850G>A , CM000680.1:g.56116850G>A GRCh37
NC_000018.8:g.54267830G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.857G>A
NR_170243.1:n.307+78G>A
NR_170244.1:n.307+78G>A
NR_170245.1:n.307+78G>A
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