Canonical Allele Identifier: CA621140282
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs1338121414
gnomAD v2: 16-14395272-CA-C
gnomAD v3: 16-14301415-CA-C
gnomAD v4: 16-14301415-CA-C
MyVariant Identifiers: chr16:g.14395273del (hg19) chr16:g.14301416del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301417del , CM000678.2:g.14301417del GRCh38
NC_000016.9:g.14395274del , CM000678.1:g.14395274del GRCh37
NC_000016.8:g.14302775del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.37del
Search 100 bp 5'
Search 100 bp 3'