Canonical Allele Identifier: CA2209242000
Gene: MIR193BHG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301410A= , CM000678.2:g.14301410A= GRCh38
NC_000016.9:g.14395267A= , CM000678.1:g.14395267A= GRCh37
NC_000016.8:g.14302768A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.30A=