Canonical Allele Identifier: CA746165521

Gene: MIR646HG

Linked Data

• dbSNP Id: rs1318589191
• MyVariant Identifiers: chr20:g.58895528A>T (hg19) ; chr20:g.60320470A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.60320470A>T , CM000682.2:g.60320470A>T	GRCh38
NC_000020.10:g.58895528A>T , CM000682.1:g.58895528A>T	GRCh37
NC_000020.9:g.58328923A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046099.1:n.420-163A>T