Canonical Allele Identifier: CA746165574
Gene: MIR646HG HGNC NCBI

Linked Data

dbSNP Id: rs1212885416
MyVariant Identifiers: chr20:g.58895639T>G (hg19) chr20:g.60320581T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320581T>G , CM000682.2:g.60320581T>G GRCh38
NC_000020.10:g.58895639T>G , CM000682.1:g.58895639T>G GRCh37
NC_000020.9:g.58329034T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.420-52T>G
Search 100 bp 5'
Search 100 bp 3'