Canonical Allele Identifier: CA511291556

Gene: MIR646HG

Linked Data

• dbSNP Id: rs1037385043
• MyVariant Identifiers: chr20:g.58895918T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.60320860T>A , CM000682.2:g.60320860T>A	GRCh38
NC_000020.10:g.58895918T>A , CM000682.1:g.58895918T>A	GRCh37
NC_000020.9:g.58329313T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046099.1:n.647T>A