Canonical Allele Identifier: CA511291139
Gene: MIR646HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.58895772C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320714C>G , CM000682.2:g.60320714C>G GRCh38
NC_000020.10:g.58895772C>G , CM000682.1:g.58895772C>G GRCh37
NC_000020.9:g.58329167C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.501C>G