Canonical Allele Identifier: CA2631848251
Gene: MIR193BHG HGNC NCBI

Linked Data

gnomAD v4: 16-14301398-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301398C>T , CM000678.2:g.14301398C>T GRCh38
NC_000016.9:g.14395255C>T , CM000678.1:g.14395255C>T GRCh37
NC_000016.8:g.14302756C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_170633.1:n.18C>T
Search 100 bp 5'
Search 100 bp 3'