Canonical Allele Identifier: CA621140281
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs1396161999

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301400G>C , CM000678.2:g.14301400G>C GRCh38
NC_000016.9:g.14395257G>C , CM000678.1:g.14395257G>C GRCh37
NC_000016.8:g.14302758G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.20G>C