Canonical Allele Identifier: CA511291116

Gene: MIR646HG

Linked Data

• dbSNP Id: rs2123093539
• MyVariant Identifiers: chr20:g.58895764T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.60320706T>G , CM000682.2:g.60320706T>G	GRCh38
NC_000020.10:g.58895764T>G , CM000682.1:g.58895764T>G	GRCh37
NC_000020.9:g.58329159T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046099.1:n.493T>G