Canonical Allele Identifier: CA990758735
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs2051157566

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449884A>C , CM000680.2:g.58449884A>C GRCh38
NC_000018.9:g.56117116A>C , CM000680.1:g.56117116A>C GRCh37
NC_000018.8:g.54268096A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1123A>C
NR_170243.1:n.307+344A>C
NR_170244.1:n.307+344A>C
NR_170245.1:n.307+344A>C