Canonical Allele Identifier: CA621140288
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs1448752914
gnomAD v2: 16-14395423-T-G
gnomAD v3: 16-14301566-T-G
gnomAD v4: 16-14301566-T-G
MyVariant Identifiers: chr16:g.14395423T>G (hg19) chr16:g.14301566T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301566T>G , CM000678.2:g.14301566T>G GRCh38
NC_000016.9:g.14395423T>G , CM000678.1:g.14395423T>G GRCh37
NC_000016.8:g.14302924T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.151+35T>G
Search 100 bp 5'
Search 100 bp 3'