Canonical Allele Identifier: CA2209242068
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs246185

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301575T>A , CM000678.2:g.14301575T>A GRCh38
NC_000016.9:g.14395432T>A , CM000678.1:g.14395432T>A GRCh37
NC_000016.8:g.14302933T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.151+44T>A