Canonical Allele Identifier: CA746165540
Gene: MIR646HG HGNC NCBI

Linked Data

dbSNP Id: rs1361390315
gnomAD v3: 20-60320506-T-C
gnomAD v4: 20-60320506-T-C
MyVariant Identifiers: chr20:g.58895564T>C (hg19) chr20:g.60320506T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320506T>C , CM000682.2:g.60320506T>C GRCh38
NC_000020.10:g.58895564T>C , CM000682.1:g.58895564T>C GRCh37
NC_000020.9:g.58328959T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.420-127T>C
Search 100 bp 5'
Search 100 bp 3'