Canonical Allele Identifier: CA300903580
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs887181223

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450006A>G , CM000680.2:g.58450006A>G GRCh38
NC_000018.9:g.56117238A>G , CM000680.1:g.56117238A>G GRCh37
NC_000018.8:g.54268218A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1245A>G
NR_170243.1:n.307+466A>G
NR_170244.1:n.307+466A>G
NR_170245.1:n.307+466A>G