Canonical Allele Identifier: CA2805953115
Gene: MIR193BHG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301597T>C , CM000678.2:g.14301597T>C GRCh38
NC_000016.9:g.14395454T>C , CM000678.1:g.14395454T>C GRCh37
NC_000016.8:g.14302955T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_170633.1:n.151+66T>C