Canonical Allele Identifier: CA504024696

Gene: MIR122HG

Linked Data

• gnomAD v4: 18-58449563-T-G
• MyVariant Identifiers: chr18:g.56116795T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58449563T>G , CM000680.2:g.58449563T>G	GRCh38
NC_000018.9:g.56116795T>G , CM000680.1:g.56116795T>G	GRCh37
NC_000018.8:g.54267775T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001753465.2:n.802T>G
NR_170243.1:n.307+23T>G
NR_170244.1:n.307+23T>G
NR_170245.1:n.307+23T>G