Canonical Allele Identifier: CA504024782

Gene: MIR122HG

Linked Data

• gnomAD v4: 18-58449578-T-C
• MyVariant Identifiers: chr18:g.56116810T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58449578T>C , CM000680.2:g.58449578T>C	GRCh38
NC_000018.9:g.56116810T>C , CM000680.1:g.56116810T>C	GRCh37
NC_000018.8:g.54267790T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001753465.2:n.817T>C
NR_170243.1:n.307+38T>C
NR_170244.1:n.307+38T>C
NR_170245.1:n.307+38T>C