Canonical Allele Identifier: CA718346228
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs570490575
gnomAD v4: 16-14301549-G-T
MyVariant Identifiers: chr16:g.14395406G>T (hg19) chr16:g.14301549G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301549G>T , CM000678.2:g.14301549G>T GRCh38
NC_000016.9:g.14395406G>T , CM000678.1:g.14395406G>T GRCh37
NC_000016.8:g.14302907G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.151+18G>T
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