Canonical Allele Identifier: CA2209242077
Gene: MIR193BHG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301589C= , CM000678.2:g.14301589C= GRCh38
NC_000016.9:g.14395446C= , CM000678.1:g.14395446C= GRCh37
NC_000016.8:g.14302947C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.151+58C=