Canonical Allele Identifier: CA2209242059
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs2044152915
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301557dup , CM000678.2:g.14301557dup GRCh38
NC_000016.9:g.14395414dup , CM000678.1:g.14395414dup GRCh37
NC_000016.8:g.14302915dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.151+26dup
Search 100 bp 5'
Search 100 bp 3'