Canonical Allele Identifier: CA718346293

Gene: MIR193BHG

Linked Data

• dbSNP Id: rs1283968176
• MyVariant Identifiers: chr16:g.14395447C>T (hg19) ; chr16:g.14301590C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14301590C>T , CM000678.2:g.14301590C>T	GRCh38
NC_000016.9:g.14395447C>T , CM000678.1:g.14395447C>T	GRCh37
NC_000016.8:g.14302948C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_170633.1:n.151+59C>T