Canonical Allele Identifier: CA2209242065
Gene: MIR193BHG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301572A= , CM000678.2:g.14301572A= GRCh38
NC_000016.9:g.14395429A= , CM000678.1:g.14395429A= GRCh37
NC_000016.8:g.14302930A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.151+41A=