Canonical Allele Identifier: CA974944285
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs2044153125
gnomAD v3: 16-14301592-A-G
gnomAD v4: 16-14301592-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301592A>G , CM000678.2:g.14301592A>G GRCh38
NC_000016.9:g.14395449A>G , CM000678.1:g.14395449A>G GRCh37
NC_000016.8:g.14302950A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170633.1:n.151+61A>G
Search 100 bp 5'
Search 100 bp 3'