Canonical Allele Identifier: CA974944282

Gene: MIR193BHG

Linked Data

• dbSNP Id: rs2044152975
• gnomAD v3: 16-14301572-A-C
• gnomAD v4: 16-14301572-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14301572A>C , CM000678.2:g.14301572A>C	GRCh38
NC_000016.9:g.14395429A>C , CM000678.1:g.14395429A>C	GRCh37
NC_000016.8:g.14302930A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_170633.1:n.151+41A>C