Canonical Allele Identifier: CA2735139296
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs2144062568

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450085dup , CM000680.2:g.58450085dup GRCh38
NC_000018.9:g.56117317dup , CM000680.1:g.56117317dup GRCh37
NC_000018.8:g.54268297dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1324dup
NR_170243.1:n.308-406dup
NR_170244.1:n.307+545dup
NR_170245.1:n.307+545dup