Canonical Allele Identifier: CA504024911
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs115325424
MyVariant Identifiers: chr18:g.56116833G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449601G>A , CM000680.2:g.58449601G>A GRCh38
NC_000018.9:g.56116833G>A , CM000680.1:g.56116833G>A GRCh37
NC_000018.8:g.54267813G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.840G>A
NR_170243.1:n.307+61G>A
NR_170244.1:n.307+61G>A
NR_170245.1:n.307+61G>A