Canonical Allele Identifier: CA630057321

Gene: MIR122HG

Linked Data

• dbSNP Id: rs1426061705
• gnomAD v2: 18-56117413-C-T
• gnomAD v3: 18-58450181-C-T
• gnomAD v4: 18-58450181-C-T
• MyVariant Identifiers: chr18:g.56117413C>T (hg19) ; chr18:g.58450181C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58450181C>T , CM000680.2:g.58450181C>T	GRCh38
NC_000018.9:g.56117413C>T , CM000680.1:g.56117413C>T	GRCh37
NC_000018.8:g.54268393C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001753465.2:n.1420C>T
NR_170243.1:n.308-310C>T
NR_170244.1:n.307+641C>T
NR_170245.1:n.308-638C>T