Canonical Allele Identifier: CA2735025696
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs944131128

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450010T>C , CM000680.2:g.58450010T>C GRCh38
NC_000018.9:g.56117242T>C , CM000680.1:g.56117242T>C GRCh37
NC_000018.8:g.54268222T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1249T>C
NR_170243.1:n.307+470T>C
NR_170244.1:n.307+470T>C
NR_170245.1:n.307+470T>C