Canonical Allele Identifier: CA511291649
Gene: MIR646HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.58895949C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320891C>T , CM000682.2:g.60320891C>T GRCh38
NC_000020.10:g.58895949C>T , CM000682.1:g.58895949C>T GRCh37
NC_000020.9:g.58329344C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.678C>T