Canonical Allele Identifier: CA511291180
Gene: MIR646HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.58895786C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320728C>T , CM000682.2:g.60320728C>T GRCh38
NC_000020.10:g.58895786C>T , CM000682.1:g.58895786C>T GRCh37
NC_000020.9:g.58329181C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.515C>T
Search 100 bp 5'
Search 100 bp 3'