Canonical Allele Identifier: CA2306457362
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs1602165935
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450029A>T , CM000680.2:g.58450029A>T GRCh38
NC_000018.9:g.56117261A>T , CM000680.1:g.56117261A>T GRCh37
NC_000018.8:g.54268241A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1268A>T
NR_170243.1:n.308-462A>T
NR_170244.1:n.307+489A>T
NR_170245.1:n.307+489A>T
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