Canonical Allele Identifier: CA504024792
Gene: MIR122HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.56116812A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449580A>T , CM000680.2:g.58449580A>T GRCh38
NC_000018.9:g.56116812A>T , CM000680.1:g.56116812A>T GRCh37
NC_000018.8:g.54267792A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.819A>T
NR_170243.1:n.307+40A>T
NR_170244.1:n.307+40A>T
NR_170245.1:n.307+40A>T
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