Canonical Allele Identifier: CA278933638

Gene: MIR193BHG

Linked Data

• dbSNP Id: rs563188724
• gnomAD v3: 16-14301432-C-T
• gnomAD v4: 16-14301432-C-T
• MyVariant Identifiers: chr16:g.14395289C>T (hg19) ; chr16:g.14301432C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14301432C>T , CM000678.2:g.14301432C>T	GRCh38
NC_000016.9:g.14395289C>T , CM000678.1:g.14395289C>T	GRCh37
NC_000016.8:g.14302790C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_170633.1:n.52C>T