Canonical Allele Identifier: CA780908177

Gene: MIR122HG

Linked Data

• dbSNP Id: rs1436115706
• gnomAD v3: 18-58449679-G-A
• gnomAD v4: 18-58449679-G-A
• MyVariant Identifiers: chr18:g.56116911G>A (hg19) ; chr18:g.58449679G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58449679G>A , CM000680.2:g.58449679G>A	GRCh38
NC_000018.9:g.56116911G>A , CM000680.1:g.56116911G>A	GRCh37
NC_000018.8:g.54267891G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001753465.2:n.918G>A
NR_170243.1:n.307+139G>A
NR_170244.1:n.307+139G>A
NR_170245.1:n.307+139G>A