Canonical Allele Identifier: CA1081639500
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1751412284
gnomAD v3: 5-132350166-CAA-C
gnomAD v4: 5-132350166-CAA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350167_132350168del , CM000667.2:g.132350167_132350168del GRCh38
NC_000005.9:g.131685860_131685861del , CM000667.1:g.131685860_131685861del GRCh37
NC_000005.8:g.131713759_131713760del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.418-211_418-210del
Search 100 bp 5'
Search 100 bp 3'