Canonical Allele Identifier: CA718346211
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs1387826777
gnomAD v3: 16-14301531-G-A
gnomAD v4: 16-14301531-G-A
MyVariant Identifiers: chr16:g.14395388G>A (hg19) chr16:g.14301531G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301531G>A , CM000678.2:g.14301531G>A GRCh38
NC_000016.9:g.14395388G>A , CM000678.1:g.14395388G>A GRCh37
NC_000016.8:g.14302889G>A NCBI36

Transcript Alleles

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