Canonical Allele Identifier: CA2306457184
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs1602165782

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449633A>G , CM000680.2:g.58449633A>G GRCh38
NC_000018.9:g.56116865A>G , CM000680.1:g.56116865A>G GRCh37
NC_000018.8:g.54267845A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.872A>G
NR_170243.1:n.307+93A>G
NR_170244.1:n.307+93A>G
NR_170245.1:n.307+93A>G