Canonical Allele Identifier: CA630396158
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs1216304010
gnomAD v2: 18-56116935-T-C
gnomAD v3: 18-58449703-T-C
gnomAD v4: 18-58449703-T-C
MyVariant Identifiers: chr18:g.56116935T>C (hg19) chr18:g.58449703T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449703T>C , CM000680.2:g.58449703T>C GRCh38
NC_000018.9:g.56116935T>C , CM000680.1:g.56116935T>C GRCh37
NC_000018.8:g.54267915T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.942T>C
NR_170243.1:n.307+163T>C
NR_170244.1:n.307+163T>C
NR_170245.1:n.307+163T>C
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