Canonical Allele Identifier: CA2209242019
Gene: MIR193BHG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301468A= , CM000678.2:g.14301468A= GRCh38
NC_000016.9:g.14395325A= , CM000678.1:g.14395325A= GRCh37
NC_000016.8:g.14302826A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.88A=