Canonical Allele Identifier: CA990758634
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs2051156022

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449643A>G , CM000680.2:g.58449643A>G GRCh38
NC_000018.9:g.56116875A>G , CM000680.1:g.56116875A>G GRCh37
NC_000018.8:g.54267855A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.882A>G
NR_170243.1:n.307+103A>G
NR_170244.1:n.307+103A>G
NR_170245.1:n.307+103A>G