Canonical Allele Identifier: CA2373187675
Gene: MIR646HG HGNC NCBI

Linked Data

dbSNP Id: rs1981174411

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320518T>A , CM000682.2:g.60320518T>A GRCh38
NC_000020.10:g.58895576T>A , CM000682.1:g.58895576T>A GRCh37
NC_000020.9:g.58328971T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.420-115T>A