Canonical Allele Identifier: CA2631848419
Gene: MIR193BHG HGNC NCBI

Linked Data

gnomAD v4: 16-14301601-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301601G>T , CM000678.2:g.14301601G>T GRCh38
NC_000016.9:g.14395458G>T , CM000678.1:g.14395458G>T GRCh37
NC_000016.8:g.14302959G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_170633.1:n.151+70G>T
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