Canonical Allele Identifier: CA2209242099

Gene: MIR193BHG

Linked Data

• dbSNP Id: rs2044153324
• gnomAD v4: 16-14301615-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14301615G>T , CM000678.2:g.14301615G>T	GRCh38
NC_000016.9:g.14395472G>T , CM000678.1:g.14395472G>T	GRCh37
NC_000016.8:g.14302973G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_170633.1:n.151+84G>T