Canonical Allele Identifier: CA511291413

Gene: MIR646HG

Linked Data

• gnomAD v4: 20-60320810-T-C
• MyVariant Identifiers: chr20:g.58895868T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.60320810T>C , CM000682.2:g.60320810T>C	GRCh38
NC_000020.10:g.58895868T>C , CM000682.1:g.58895868T>C	GRCh37
NC_000020.9:g.58329263T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046099.1:n.597T>C