Canonical Allele Identifier: CA974944276
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs2044152833
gnomAD v3: 16-14301529-G-A
gnomAD v4: 16-14301529-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301529G>A , CM000678.2:g.14301529G>A GRCh38
NC_000016.9:g.14395386G>A , CM000678.1:g.14395386G>A GRCh37
NC_000016.8:g.14302887G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_170633.1:n.149G>A
Search 100 bp 5'
Search 100 bp 3'