Canonical Allele Identifier: CA2306457385
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs1201024816

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450070T>A , CM000680.2:g.58450070T>A GRCh38
NC_000018.9:g.56117302T>A , CM000680.1:g.56117302T>A GRCh37
NC_000018.8:g.54268282T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1309T>A
NR_170243.1:n.308-421T>A
NR_170244.1:n.307+530T>A
NR_170245.1:n.307+530T>A