Canonical Allele Identifier: CA990758956
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs2051159424

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450136A>T , CM000680.2:g.58450136A>T GRCh38
NC_000018.9:g.56117368A>T , CM000680.1:g.56117368A>T GRCh37
NC_000018.8:g.54268348A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1375A>T
NR_170243.1:n.308-355A>T
NR_170244.1:n.307+596A>T
NR_170245.1:n.307+596A>T