Canonical Allele Identifier: CA504025031
Gene: MIR122HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.56116855A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449623A>C , CM000680.2:g.58449623A>C GRCh38
NC_000018.9:g.56116855A>C , CM000680.1:g.56116855A>C GRCh37
NC_000018.8:g.54267835A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.862A>C
NR_170243.1:n.307+83A>C
NR_170244.1:n.307+83A>C
NR_170245.1:n.307+83A>C