Canonical Allele Identifier: CA2373187821
Gene: MIR646HG HGNC NCBI

Linked Data

dbSNP Id: rs1981185932

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320895_60320896del , CM000682.2:g.60320895_60320896del GRCh38
NC_000020.10:g.58895953_58895954del , CM000682.1:g.58895953_58895954del GRCh37
NC_000020.9:g.58329348_58329349del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.682_683del