Canonical Allele Identifier: CA317000029
Gene: MIR646HG HGNC NCBI

Linked Data

dbSNP Id: rs547048500

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320476A>G , CM000682.2:g.60320476A>G GRCh38
NC_000020.10:g.58895534A>G , CM000682.1:g.58895534A>G GRCh37
NC_000020.9:g.58328929A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.420-157A>G