Canonical Allele Identifier: CA718346112

Gene: MIR193BHG

Linked Data

• dbSNP Id: rs1308539578
• gnomAD v4: 16-14301398-C-A
• MyVariant Identifiers: chr16:g.14395255C>A (hg19) ; chr16:g.14301398C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14301398C>A , CM000678.2:g.14301398C>A	GRCh38
NC_000016.9:g.14395255C>A , CM000678.1:g.14395255C>A	GRCh37
NC_000016.8:g.14302756C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_170633.1:n.18C>A