Canonical Allele Identifier: CA718346146

Gene: MIR193BHG

Linked Data

• dbSNP Id: rs1404387639
• gnomAD v4: 16-14301407-A-G
• MyVariant Identifiers: chr16:g.14395264A>G (hg19) ; chr16:g.14301407A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14301407A>G , CM000678.2:g.14301407A>G	GRCh38
NC_000016.9:g.14395264A>G , CM000678.1:g.14395264A>G	GRCh37
NC_000016.8:g.14302765A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_170633.1:n.27A>G