Canonical Allele Identifier: CA2306457366
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs1602165938

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450047T>C , CM000680.2:g.58450047T>C GRCh38
NC_000018.9:g.56117279T>C , CM000680.1:g.56117279T>C GRCh37
NC_000018.8:g.54268259T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1286T>C
NR_170243.1:n.308-444T>C
NR_170244.1:n.307+507T>C
NR_170245.1:n.307+507T>C