Canonical Allele Identifier: CA2373187682
Gene: MIR646HG HGNC NCBI

Linked Data

dbSNP Id: rs1568694012

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320526A>G , CM000682.2:g.60320526A>G GRCh38
NC_000020.10:g.58895584A>G , CM000682.1:g.58895584A>G GRCh37
NC_000020.9:g.58328979A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.420-107A>G