Canonical Allele Identifier: CA621140289
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs1291872995

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301576del , CM000678.2:g.14301576del GRCh38
NC_000016.9:g.14395433del , CM000678.1:g.14395433del GRCh37
NC_000016.8:g.14302934del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.151+45del