Canonical Allele Identifier: CA504024632

Gene: MIR122HG

Linked Data

• gnomAD v4: 18-58449552-A-G
• MyVariant Identifiers: chr18:g.56116784A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58449552A>G , CM000680.2:g.58449552A>G	GRCh38
NC_000018.9:g.56116784A>G , CM000680.1:g.56116784A>G	GRCh37
NC_000018.8:g.54267764A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001753465.2:n.791A>G
NR_170243.1:n.307+12A>G
NR_170244.1:n.307+12A>G
NR_170245.1:n.307+12A>G