Canonical Allele Identifier: CA511291632
Gene: MIR646HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.58895944T>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320886T>A , CM000682.2:g.60320886T>A GRCh38
NC_000020.10:g.58895944T>A , CM000682.1:g.58895944T>A GRCh37
NC_000020.9:g.58329339T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.673T>A
Search 100 bp 5'
Search 100 bp 3'