Canonical Allele Identifier: CA974944275
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs2044152737

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301504C>T , CM000678.2:g.14301504C>T GRCh38
NC_000016.9:g.14395361C>T , CM000678.1:g.14395361C>T GRCh37
NC_000016.8:g.14302862C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_170633.1:n.124C>T