Canonical Allele Identifier: CA14519270
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs9966765

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449558C>G , CM000680.2:g.58449558C>G GRCh38
NC_000018.9:g.56116790C>G , CM000680.1:g.56116790C>G GRCh37
NC_000018.8:g.54267770C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001753465.2:n.797C>G
NR_170243.1:n.307+18C>G
NR_170244.1:n.307+18C>G
NR_170245.1:n.307+18C>G