Canonical Allele Identifier: CA2209242035
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs2044152718

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301502dup , CM000678.2:g.14301502dup GRCh38
NC_000016.9:g.14395359dup , CM000678.1:g.14395359dup GRCh37
NC_000016.8:g.14302860dup NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_170633.1:n.122dup