Canonical Allele Identifier: CA2209242001
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs2044152404

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301410A>C , CM000678.2:g.14301410A>C GRCh38
NC_000016.9:g.14395267A>C , CM000678.1:g.14395267A>C GRCh37
NC_000016.8:g.14302768A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.30A>C