Canonical Allele Identifier: CA2805953116
Gene: MIR193BHG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301602T>G , CM000678.2:g.14301602T>G GRCh38
NC_000016.9:g.14395459T>G , CM000678.1:g.14395459T>G GRCh37
NC_000016.8:g.14302960T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.151+71T>G