Canonical Allele Identifier: CA317000050
Gene: MIR646HG HGNC NCBI

Linked Data

dbSNP Id: rs996057186
gnomAD v2: 20-58895768-T-C
gnomAD v3: 20-60320710-T-C
gnomAD v4: 20-60320710-T-C
MyVariant Identifiers: chr20:g.58895768T>C (hg19) chr20:g.60320710T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320710T>C , CM000682.2:g.60320710T>C GRCh38
NC_000020.10:g.58895768T>C , CM000682.1:g.58895768T>C GRCh37
NC_000020.9:g.58329163T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.497T>C
Search 100 bp 5'
Search 100 bp 3'