Canonical Allele Identifier: CA15867217

Gene: MIR193BHG

Linked Data

• dbSNP Id: rs246185
• gnomAD v2: 16-14395432-T-C
• gnomAD v3: 16-14301575-T-C
• gnomAD v4: 16-14301575-T-C
• MyVariant Identifiers: chr16:g.14395432T>C (hg19) ; chr16:g.14395432_14395433delinsCG (hg19) ; chr16:g.14301575T>C (hg38) ; chr16:g.14301575_14301576delinsCG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14301575T>C , CM000678.2:g.14301575T>C	GRCh38
NC_000016.9:g.14395432T>C , CM000678.1:g.14395432T>C	GRCh37
NC_000016.8:g.14302933T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_170633.1:n.151+44T>C