Canonical Allele Identifier: CA278933646
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs975035267
MyVariant Identifiers: chr16:g.14395369C>T (hg19) chr16:g.14301512C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301512C>T , CM000678.2:g.14301512C>T GRCh38
NC_000016.9:g.14395369C>T , CM000678.1:g.14395369C>T GRCh37
NC_000016.8:g.14302870C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.132C>T
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Search 100 bp 3'