Canonical Allele Identifier: CA746165539
Gene: MIR646HG HGNC NCBI

Linked Data

dbSNP Id: rs1415585782

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320501T>C , CM000682.2:g.60320501T>C GRCh38
NC_000020.10:g.58895559T>C , CM000682.1:g.58895559T>C GRCh37
NC_000020.9:g.58328954T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.420-132T>C