Canonical Allele Identifier: CA1583137303
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1751790622
gnomAD v4: 5-132369537-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369537C>A , CM000667.2:g.132369537C>A GRCh38
NC_000005.9:g.131705229C>A , CM000667.1:g.131705229C>A GRCh37
NC_000005.8:g.131733128C>A NCBI36
NG_008982.1:g.4829C>A
NG_008982.2:g.4834C>A

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+307G>T
Search 100 bp 5'
Search 100 bp 3'