Canonical Allele Identifier: CA511290929

Gene: MIR646HG

Linked Data

• gnomAD v4: 20-60320644-C-T
• MyVariant Identifiers: chr20:g.58895702C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.60320644C>T , CM000682.2:g.60320644C>T	GRCh38
NC_000020.10:g.58895702C>T , CM000682.1:g.58895702C>T	GRCh37
NC_000020.9:g.58329097C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046099.1:n.431C>T