Canonical Allele Identifier: CA2373187831
Gene: MIR646HG HGNC NCBI

Linked Data

dbSNP Id: rs1981186848

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320934_60320935del , CM000682.2:g.60320934_60320935del GRCh38
NC_000020.10:g.58895992_58895993del , CM000682.1:g.58895992_58895993del GRCh37
NC_000020.9:g.58329387_58329388del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.721_722del