Canonical Allele Identifier: CA718346291

Gene: MIR193BHG

Linked Data

• dbSNP Id: rs1247640989
• MyVariant Identifiers: chr16:g.14395446C>G (hg19) ; chr16:g.14301589C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14301589C>G , CM000678.2:g.14301589C>G	GRCh38
NC_000016.9:g.14395446C>G , CM000678.1:g.14395446C>G	GRCh37
NC_000016.8:g.14302947C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_170633.1:n.151+58C>G