Canonical Allele Identifier: CA974944286
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs2044153143

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301594T>C , CM000678.2:g.14301594T>C GRCh38
NC_000016.9:g.14395451T>C , CM000678.1:g.14395451T>C GRCh37
NC_000016.8:g.14302952T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_170633.1:n.151+63T>C