Canonical Allele Identifier: CA511291492
Gene: MIR646HG HGNC NCBI

Linked Data

dbSNP Id: rs1981184331
MyVariant Identifiers: chr20:g.58895897C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320839C>A , CM000682.2:g.60320839C>A GRCh38
NC_000020.10:g.58895897C>A , CM000682.1:g.58895897C>A GRCh37
NC_000020.9:g.58329292C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.626C>A