Canonical Allele Identifier: CA504024666
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs9966765
COSMIC: COSN9339196 COSN15419015 COSN15467650 COSN15483152
MyVariant Identifiers: chr18:g.56116790C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449558C>A , CM000680.2:g.58449558C>A GRCh38
NC_000018.9:g.56116790C>A , CM000680.1:g.56116790C>A GRCh37
NC_000018.8:g.54267770C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001753465.2:n.797C>A
NR_170243.1:n.307+18C>A
NR_170244.1:n.307+18C>A
NR_170245.1:n.307+18C>A
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