Canonical Allele Identifier: CA504024602
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs1482431953
gnomAD v2: 18-56116779-C-A
gnomAD v3: 18-58449547-C-A
gnomAD v4: 18-58449547-C-A
MyVariant Identifiers: chr18:g.56116779C>A (hg19) chr18:g.58449547C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449547C>A , CM000680.2:g.58449547C>A GRCh38
NC_000018.9:g.56116779C>A , CM000680.1:g.56116779C>A GRCh37
NC_000018.8:g.54267759C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.786C>A
NR_170243.1:n.307+7C>A
NR_170244.1:n.307+7C>A
NR_170245.1:n.307+7C>A
Search 100 bp 5'
Search 100 bp 3'