Canonical Allele Identifier: CA630057311

Gene: MIR122HG

Linked Data

• dbSNP Id: rs1297105464
• gnomAD v2: 18-56117181-G-C
• gnomAD v3: 18-58449949-G-C
• gnomAD v4: 18-58449949-G-C
• MyVariant Identifiers: chr18:g.56117181G>C (hg19) ; chr18:g.58449949G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58449949G>C , CM000680.2:g.58449949G>C	GRCh38
NC_000018.9:g.56117181G>C , CM000680.1:g.56117181G>C	GRCh37
NC_000018.8:g.54268161G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001753465.2:n.1188G>C
NR_170243.1:n.307+409G>C
NR_170244.1:n.307+409G>C
NR_170245.1:n.307+409G>C