Canonical Allele Identifier: CA511291124

Gene: MIR646HG

Linked Data

• dbSNP Id: rs1246815875
• gnomAD v2: 20-58895767-A-C
• gnomAD v3: 20-60320709-A-C
• gnomAD v4: 20-60320709-A-C
• MyVariant Identifiers: chr20:g.58895767A>C (hg19) ; chr20:g.60320709A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.60320709A>C , CM000682.2:g.60320709A>C	GRCh38
NC_000020.10:g.58895767A>C , CM000682.1:g.58895767A>C	GRCh37
NC_000020.9:g.58329162A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046099.1:n.496A>C