Canonical Allele Identifier: CA2306457387
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs1602165971
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450071T>A , CM000680.2:g.58450071T>A GRCh38
NC_000018.9:g.56117303T>A , CM000680.1:g.56117303T>A GRCh37
NC_000018.8:g.54268283T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1310T>A
NR_170243.1:n.308-420T>A
NR_170244.1:n.307+531T>A
NR_170245.1:n.307+531T>A
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