Canonical Allele Identifier: CA2653579474
Gene: MIR646HG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320547A>T , CM000682.2:g.60320547A>T GRCh38
NC_000020.10:g.58895605A>T , CM000682.1:g.58895605A>T GRCh37
NC_000020.9:g.58329000A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.420-86A>T