Canonical Allele Identifier: CA300903659
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs997138019

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450061A>G , CM000680.2:g.58450061A>G GRCh38
NC_000018.9:g.56117293A>G , CM000680.1:g.56117293A>G GRCh37
NC_000018.8:g.54268273A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1300A>G
NR_170243.1:n.308-430A>G
NR_170244.1:n.307+521A>G
NR_170245.1:n.307+521A>G