Canonical Allele Identifier: CA621140293
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs1175901873

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301620G>C , CM000678.2:g.14301620G>C GRCh38
NC_000016.9:g.14395477G>C , CM000678.1:g.14395477G>C GRCh37
NC_000016.8:g.14302978G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.151+89G>C