Canonical Allele Identifier: CA2306457202
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs2051156174

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449663_58449668del , CM000680.2:g.58449663_58449668del GRCh38
NC_000018.9:g.56116895_56116900del , CM000680.1:g.56116895_56116900del GRCh37
NC_000018.8:g.54267875_54267880del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.902_907del
NR_170243.1:n.307+123_307+128del
NR_170244.1:n.307+123_307+128del
NR_170245.1:n.307+123_307+128del