Canonical Allele Identifier: CA504024937
Gene: MIR122HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.56116838G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449606G>C , CM000680.2:g.58449606G>C GRCh38
NC_000018.9:g.56116838G>C , CM000680.1:g.56116838G>C GRCh37
NC_000018.8:g.54267818G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.845G>C
NR_170243.1:n.307+66G>C
NR_170244.1:n.307+66G>C
NR_170245.1:n.307+66G>C