Canonical Allele Identifier: CA2631848432
Gene: MIR193BHG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301626T>G , CM000678.2:g.14301626T>G GRCh38
NC_000016.9:g.14395483T>G , CM000678.1:g.14395483T>G GRCh37
NC_000016.8:g.14302984T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.151+95T>G