Canonical Allele Identifier: CA511290895
Gene: MIR646HG HGNC NCBI

Linked Data

dbSNP Id: rs1981177335
gnomAD v3: 20-60320629-C-T
gnomAD v4: 20-60320629-C-T
MyVariant Identifiers: chr20:g.58895687C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320629C>T , CM000682.2:g.60320629C>T GRCh38
NC_000020.10:g.58895687C>T , CM000682.1:g.58895687C>T GRCh37
NC_000020.9:g.58329082C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.420-4C>T
Search 100 bp 5'
Search 100 bp 3'