Canonical Allele Identifier: CA504024908
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs2051155785
MyVariant Identifiers: chr18:g.56116832A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449600A>G , CM000680.2:g.58449600A>G GRCh38
NC_000018.9:g.56116832A>G , CM000680.1:g.56116832A>G GRCh37
NC_000018.8:g.54267812A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.839A>G
NR_170243.1:n.307+60A>G
NR_170244.1:n.307+60A>G
NR_170245.1:n.307+60A>G