Canonical Allele Identifier: CA2209242108
Gene: MIR193BHG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301629T= , CM000678.2:g.14301629T= GRCh38
NC_000016.9:g.14395486T= , CM000678.1:g.14395486T= GRCh37
NC_000016.8:g.14302987T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.151+98T=