Canonical Allele Identifier: CA621140286
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs1483694303

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301524C>T , CM000678.2:g.14301524C>T GRCh38
NC_000016.9:g.14395381C>T , CM000678.1:g.14395381C>T GRCh37
NC_000016.8:g.14302882C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.144C>T