Canonical Allele Identifier: CA746165534
Gene: MIR646HG HGNC NCBI

Linked Data

dbSNP Id: rs1353858839
gnomAD v3: 20-60320475-A-C
gnomAD v4: 20-60320475-A-C
MyVariant Identifiers: chr20:g.58895533A>C (hg19) chr20:g.60320475A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320475A>C , CM000682.2:g.60320475A>C GRCh38
NC_000020.10:g.58895533A>C , CM000682.1:g.58895533A>C GRCh37
NC_000020.9:g.58328928A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.420-158A>C
Search 100 bp 5'
Search 100 bp 3'