Canonical Allele Identifier: CA511291097
Gene: MIR646HG HGNC NCBI

Linked Data

dbSNP Id: rs1981179360
MyVariant Identifiers: chr20:g.58895758A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320700A>G , CM000682.2:g.60320700A>G GRCh38
NC_000020.10:g.58895758A>G , CM000682.1:g.58895758A>G GRCh37
NC_000020.9:g.58329153A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046099.1:n.487A>G