Canonical Allele Identifier: CA2631848421
Gene: MIR193BHG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301609A>T , CM000678.2:g.14301609A>T GRCh38
NC_000016.9:g.14395466A>T , CM000678.1:g.14395466A>T GRCh37
NC_000016.8:g.14302967A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.151+78A>T