Canonical Allele Identifier: CA2306457386
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs1602165971

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450071T>G , CM000680.2:g.58450071T>G GRCh38
NC_000018.9:g.56117303T>G , CM000680.1:g.56117303T>G GRCh37
NC_000018.8:g.54268283T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1310T>G
NR_170243.1:n.308-420T>G
NR_170244.1:n.307+531T>G
NR_170245.1:n.307+531T>G