Canonical Allele Identifier: CA2373187672
Gene: MIR646HG HGNC NCBI

Linked Data

dbSNP Id: rs1981174285

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320513G>C , CM000682.2:g.60320513G>C GRCh38
NC_000020.10:g.58895571G>C , CM000682.1:g.58895571G>C GRCh37
NC_000020.9:g.58328966G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.420-120G>C