Canonical Allele Identifier: CA780908222
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs1436534105
MyVariant Identifiers: chr18:g.56117045A>G (hg19) chr18:g.58449813A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449813A>G , CM000680.2:g.58449813A>G GRCh38
NC_000018.9:g.56117045A>G , CM000680.1:g.56117045A>G GRCh37
NC_000018.8:g.54268025A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1052A>G
NR_170243.1:n.307+273A>G
NR_170244.1:n.307+273A>G
NR_170245.1:n.307+273A>G
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