Canonical Allele Identifier: CA2209242078
Gene: MIR193BHG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301589_14301592delinsCCTA , CM000678.2:g.14301589_14301592delinsCCTA GRCh38
NC_000016.9:g.14395446_14395449delinsCCTA , CM000678.1:g.14395446_14395449delinsCCTA GRCh37
NC_000016.8:g.14302947_14302950delinsCCTA NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_170633.1:n.151+58_151+61delinsCCTA