Canonical Allele Identifier: CA504024527

Gene: MIR122HG

Linked Data

• MyVariant Identifiers: chr18:g.56116766A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58449534A>C , CM000680.2:g.58449534A>C	GRCh38
NC_000018.9:g.56116766A>C , CM000680.1:g.56116766A>C	GRCh37
NC_000018.8:g.54267746A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001753465.2:n.773A>C
NR_170243.1:n.301A>C
NR_170244.1:n.301A>C
NR_170245.1:n.301A>C