Canonical Allele Identifier: CA317000033
Gene: MIR646HG HGNC NCBI

Linked Data

dbSNP Id: rs933261786
gnomAD v3: 20-60320545-A-G
gnomAD v4: 20-60320545-A-G
MyVariant Identifiers: chr20:g.58895603A>G (hg19) chr20:g.60320545A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320545A>G , CM000682.2:g.60320545A>G GRCh38
NC_000020.10:g.58895603A>G , CM000682.1:g.58895603A>G GRCh37
NC_000020.9:g.58328998A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.420-88A>G
Search 100 bp 5'
Search 100 bp 3'