Canonical Allele Identifier: CA511291163
Gene: MIR646HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.58895780T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320722T>C , CM000682.2:g.60320722T>C GRCh38
NC_000020.10:g.58895780T>C , CM000682.1:g.58895780T>C GRCh37
NC_000020.9:g.58329175T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.509T>C