Canonical Allele Identifier: CA621140285
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs1282800390

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301520A>G , CM000678.2:g.14301520A>G GRCh38
NC_000016.9:g.14395377A>G , CM000678.1:g.14395377A>G GRCh37
NC_000016.8:g.14302878A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.140A>G