Canonical Allele Identifier: CA278933655
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs746098500
gnomAD v3: 16-14301616-TTGTG-T
gnomAD v4: 16-14301616-TTGTG-T
MyVariant Identifiers: chr16:g.14395474_14395477del (hg19) chr16:g.14301617_14301620del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301622_14301625del , CM000678.2:g.14301622_14301625del GRCh38
NC_000016.9:g.14395479_14395482del , CM000678.1:g.14395479_14395482del GRCh37
NC_000016.8:g.14302980_14302983del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.151+91_151+94del
Search 100 bp 5'
Search 100 bp 3'