Canonical Allele Identifier: CA2209242091
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs2044153213

Genomic Alleles

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

Transcript Alleles

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