Canonical Allele Identifier: CA990758721
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs2051157313

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449847T>A , CM000680.2:g.58449847T>A GRCh38
NC_000018.9:g.56117079T>A , CM000680.1:g.56117079T>A GRCh37
NC_000018.8:g.54268059T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1086T>A
NR_170243.1:n.307+307T>A
NR_170244.1:n.307+307T>A
NR_170245.1:n.307+307T>A