Canonical Allele Identifier: CA2306457425
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs2051159461

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450154T>G , CM000680.2:g.58450154T>G GRCh38
NC_000018.9:g.56117386T>G , CM000680.1:g.56117386T>G GRCh37
NC_000018.8:g.54268366T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1393T>G
NR_170243.1:n.308-337T>G
NR_170244.1:n.307+614T>G
NR_170245.1:n.307+614T>G