Canonical Allele Identifier: CA278933637

Gene: MIR193BHG

Linked Data

• dbSNP Id: rs982410254
• gnomAD v3: 16-14301406-G-A
• gnomAD v4: 16-14301406-G-A
• MyVariant Identifiers: chr16:g.14395263G>A (hg19) ; chr16:g.14301406G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14301406G>A , CM000678.2:g.14301406G>A	GRCh38
NC_000016.9:g.14395263G>A , CM000678.1:g.14395263G>A	GRCh37
NC_000016.8:g.14302764G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_170633.1:n.26G>A