Canonical Allele Identifier: CA2209242074
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs2044153067
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301584C>G , CM000678.2:g.14301584C>G GRCh38
NC_000016.9:g.14395441C>G , CM000678.1:g.14395441C>G GRCh37
NC_000016.8:g.14302942C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.151+53C>G
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