Canonical Allele Identifier: CA504024557

Gene: MIR122HG

Linked Data

• dbSNP Id: rs1602165741
• gnomAD v4: 18-58449539-T-C
• MyVariant Identifiers: chr18:g.56116771T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58449539T>C , CM000680.2:g.58449539T>C	GRCh38
NC_000018.9:g.56116771T>C , CM000680.1:g.56116771T>C	GRCh37
NC_000018.8:g.54267751T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001753465.2:n.778T>C
NR_170243.1:n.306T>C
NR_170244.1:n.306T>C
NR_170245.1:n.306T>C