Canonical Allele Identifier: CA511291405
Gene: MIR646HG HGNC NCBI

Linked Data

dbSNP Id: rs1981183079
MyVariant Identifiers: chr20:g.58895865G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320807G>C , CM000682.2:g.60320807G>C GRCh38
NC_000020.10:g.58895865G>C , CM000682.1:g.58895865G>C GRCh37
NC_000020.9:g.58329260G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.594G>C