Canonical Allele Identifier: CA504025027
Gene: MIR122HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.56116854G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449622G>T , CM000680.2:g.58449622G>T GRCh38
NC_000018.9:g.56116854G>T , CM000680.1:g.56116854G>T GRCh37
NC_000018.8:g.54267834G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.861G>T
NR_170243.1:n.307+82G>T
NR_170244.1:n.307+82G>T
NR_170245.1:n.307+82G>T