Canonical Allele Identifier: CA1019006071
Gene: MIR646HG HGNC NCBI

Linked Data

dbSNP Id: rs1981174174

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320503A>G , CM000682.2:g.60320503A>G GRCh38
NC_000020.10:g.58895561A>G , CM000682.1:g.58895561A>G GRCh37
NC_000020.9:g.58328956A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.420-130A>G