Canonical Allele Identifier: CA1081639539
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1263876993
gnomAD v3: 5-132350341-T-A
gnomAD v4: 5-132350341-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350341T>A , CM000667.2:g.132350341T>A GRCh38
NC_000005.9:g.131686034T>A , CM000667.1:g.131686034T>A GRCh37
NC_000005.8:g.131713933T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110997.1:n.418-384A>T
Search 100 bp 5'
Search 100 bp 3'