Canonical Allele Identifier: CA504024505

Gene: MIR122HG

Linked Data

• dbSNP Id: rs914439425
• MyVariant Identifiers: chr18:g.56116762C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58449530C>G , CM000680.2:g.58449530C>G	GRCh38
NC_000018.9:g.56116762C>G , CM000680.1:g.56116762C>G	GRCh37
NC_000018.8:g.54267742C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001753465.2:n.769C>G
NR_170243.1:n.297C>G
NR_170244.1:n.297C>G
NR_170245.1:n.297C>G