Canonical Allele Identifier: CA2306457383
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs10605417

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450078_58450084del , CM000680.2:g.58450078_58450084del GRCh38
NC_000018.9:g.56117310_56117316del , CM000680.1:g.56117310_56117316del GRCh37
NC_000018.8:g.54268290_54268296del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1317_1323del
NR_170243.1:n.308-413_308-407del
NR_170244.1:n.307+538_307+544del
NR_170245.1:n.307+538_307+544del