Canonical Allele Identifier: CA718346334

Gene: MIR193BHG

Linked Data

• dbSNP Id: rs1162407215
• MyVariant Identifiers: chr16:g.14395479G>C (hg19) ; chr16:g.14301622G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14301622G>C , CM000678.2:g.14301622G>C	GRCh38
NC_000016.9:g.14395479G>C , CM000678.1:g.14395479G>C	GRCh37
NC_000016.8:g.14302980G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_170633.1:n.151+91G>C