Canonical Allele Identifier: CA2631848347
Gene: MIR193BHG HGNC NCBI

Linked Data

gnomAD v4: 16-14301513-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301513T>C , CM000678.2:g.14301513T>C GRCh38
NC_000016.9:g.14395370T>C , CM000678.1:g.14395370T>C GRCh37
NC_000016.8:g.14302871T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.133T>C
Search 100 bp 5'
Search 100 bp 3'