Canonical Allele Identifier: CA2209242085
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs2044153159
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301595T>G , CM000678.2:g.14301595T>G GRCh38
NC_000016.9:g.14395452T>G , CM000678.1:g.14395452T>G GRCh37
NC_000016.8:g.14302953T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.151+64T>G
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