Canonical Allele Identifier: CA718346283

Gene: MIR193BHG

Linked Data

• dbSNP Id: rs1214384213
• gnomAD v3: 16-14301573-C-A
• gnomAD v4: 16-14301573-C-A
• MyVariant Identifiers: chr16:g.14395430C>A (hg19) ; chr16:g.14301573C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14301573C>A , CM000678.2:g.14301573C>A	GRCh38
NC_000016.9:g.14395430C>A , CM000678.1:g.14395430C>A	GRCh37
NC_000016.8:g.14302931C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_170633.1:n.151+42C>A