Canonical Allele Identifier: CA300903428
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs933190705
MyVariant Identifiers: chr18:g.56117099G>A (hg19) chr18:g.58449867G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449867G>A , CM000680.2:g.58449867G>A GRCh38
NC_000018.9:g.56117099G>A , CM000680.1:g.56117099G>A GRCh37
NC_000018.8:g.54268079G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1106G>A
NR_170243.1:n.307+327G>A
NR_170244.1:n.307+327G>A
NR_170245.1:n.307+327G>A
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