Canonical Allele Identifier: CA300903615

Gene: MIR122HG

Linked Data

• dbSNP Id: rs974434744
• MyVariant Identifiers: chr18:g.56117283C>T (hg19) ; chr18:g.58450051C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58450051C>T , CM000680.2:g.58450051C>T	GRCh38
NC_000018.9:g.56117283C>T , CM000680.1:g.56117283C>T	GRCh37
NC_000018.8:g.54268263C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001753465.2:n.1290C>T
NR_170243.1:n.308-440C>T
NR_170244.1:n.307+511C>T
NR_170245.1:n.307+511C>T