Canonical Allele Identifier: CA2209241985
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs2044152218

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301387G>A , CM000678.2:g.14301387G>A GRCh38
NC_000016.9:g.14395244G>A , CM000678.1:g.14395244G>A GRCh37
NC_000016.8:g.14302745G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.7G>A