Canonical Allele Identifier: CA2816894346
Gene: MIR646HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320528T>C , CM000682.2:g.60320528T>C GRCh38
NC_000020.10:g.58895586T>C , CM000682.1:g.58895586T>C GRCh37
NC_000020.9:g.58328981T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.420-105T>C