Canonical Allele Identifier: CA2816894341
Gene: MIR646HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320482T>C , CM000682.2:g.60320482T>C GRCh38
NC_000020.10:g.58895540T>C , CM000682.1:g.58895540T>C GRCh37
NC_000020.9:g.58328935T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.420-151T>C