Canonical Allele Identifier: CA14780699
Gene: MIR646HG HGNC NCBI

Linked Data

dbSNP Id: rs11698685
gnomAD v2: 20-58895846-G-A
gnomAD v3: 20-60320788-G-A
gnomAD v4: 20-60320788-G-A
MyVariant Identifiers: chr20:g.58895846G>A (hg19) chr20:g.60320788G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320788G>A , CM000682.2:g.60320788G>A GRCh38
NC_000020.10:g.58895846G>A , CM000682.1:g.58895846G>A GRCh37
NC_000020.9:g.58329241G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046099.1:n.575G>A
Search 100 bp 5'
Search 100 bp 3'