Canonical Allele Identifier: CA504024519

Gene: MIR122HG

Linked Data

• dbSNP Id: rs1602165737
• MyVariant Identifiers: chr18:g.56116764A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58449532A>G , CM000680.2:g.58449532A>G	GRCh38
NC_000018.9:g.56116764A>G , CM000680.1:g.56116764A>G	GRCh37
NC_000018.8:g.54267744A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001753465.2:n.771A>G
NR_170243.1:n.299A>G
NR_170244.1:n.299A>G
NR_170245.1:n.299A>G