Canonical Allele Identifier: CA300903351
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs114283594
gnomAD v2: 18-56116928-A-G
gnomAD v3: 18-58449696-A-G
gnomAD v4: 18-58449696-A-G
MyVariant Identifiers: chr18:g.56116928A>G (hg19) chr18:g.58449696A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449696A>G , CM000680.2:g.58449696A>G GRCh38
NC_000018.9:g.56116928A>G , CM000680.1:g.56116928A>G GRCh37
NC_000018.8:g.54267908A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.935A>G
NR_170243.1:n.307+156A>G
NR_170244.1:n.307+156A>G
NR_170245.1:n.307+156A>G
Search 100 bp 5'
Search 100 bp 3'