Canonical Allele Identifier: CA14780699
Gene: MIR646HG HGNC NCBI
MyVariant.info:
GRCh38 chr20:g.60320788G>A
GRCh37 chr20:g.58895846G>A
gnomAD v2:
20:58895846 G / A
gnomAD v3:
20:60320788 G / A
gnomAD v4:
chr20-60320788-G-A
Joint Max Group AF 0.36895075 (AFR)
Genomes Max Group AF 0.36893817 (AFR)
Exomes Max Group AF 0.11179019 (NFE)
dbSNP:
11698685
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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'