Canonical Allele Identifier: CA2675194545
Gene: MIR3936HG HGNC NCBI

Linked Data

gnomAD v4: 5-132369590-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369590T>A , CM000667.2:g.132369590T>A GRCh38
NC_000005.9:g.131705282T>A , CM000667.1:g.131705282T>A GRCh37
NC_000005.8:g.131733181T>A NCBI36
NG_008982.1:g.4882T>A
NG_008982.2:g.4887T>A

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+254A>T
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