Canonical Allele Identifier: CA974944301
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs2044153230
gnomAD v3: 16-14301611-G-T
gnomAD v4: 16-14301611-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301611G>T , CM000678.2:g.14301611G>T GRCh38
NC_000016.9:g.14395468G>T , CM000678.1:g.14395468G>T GRCh37
NC_000016.8:g.14302969G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.151+80G>T
Search 100 bp 5'
Search 100 bp 3'