Canonical Allele Identifier: CA718346305
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs1366211604
gnomAD v3: 16-14301610-CG-C
gnomAD v4: 16-14301610-CG-C
MyVariant Identifiers: chr16:g.14395468del (hg19) chr16:g.14301611del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301615del , CM000678.2:g.14301615del GRCh38
NC_000016.9:g.14395472del , CM000678.1:g.14395472del GRCh37
NC_000016.8:g.14302973del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.151+84del
Search 100 bp 5'
Search 100 bp 3'