Canonical Allele Identifier: CA718346294
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs1431993151
MyVariant Identifiers: chr16:g.14395457T>C (hg19) chr16:g.14301600T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301600T>C , CM000678.2:g.14301600T>C GRCh38
NC_000016.9:g.14395457T>C , CM000678.1:g.14395457T>C GRCh37
NC_000016.8:g.14302958T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.151+69T>C
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