Canonical Allele Identifier: CA621140290
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs568469678
gnomAD v2: 16-14395458-G-A
gnomAD v3: 16-14301601-G-A
gnomAD v4: 16-14301601-G-A
MyVariant Identifiers: chr16:g.14395458G>A (hg19) chr16:g.14301601G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301601G>A , CM000678.2:g.14301601G>A GRCh38
NC_000016.9:g.14395458G>A , CM000678.1:g.14395458G>A GRCh37
NC_000016.8:g.14302959G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_170633.1:n.151+70G>A
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