Canonical Allele Identifier: CA2631848357
Gene: MIR193BHG HGNC NCBI

Linked Data

gnomAD v4: 16-14301521-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301521T>C , CM000678.2:g.14301521T>C GRCh38
NC_000016.9:g.14395378T>C , CM000678.1:g.14395378T>C GRCh37
NC_000016.8:g.14302879T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_170633.1:n.141T>C
Search 100 bp 5'
Search 100 bp 3'