Canonical Allele Identifier: CA127195586
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs900895404
gnomAD v2: 5-131705223-C-G
gnomAD v3: 5-132369531-C-G
gnomAD v4: 5-132369531-C-G
MyVariant Identifiers: chr5:g.131705223C>G (hg19) chr5:g.132369531C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369531C>G , CM000667.2:g.132369531C>G GRCh38
NC_000005.9:g.131705223C>G , CM000667.1:g.131705223C>G GRCh37
NC_000005.8:g.131733122C>G NCBI36
NG_008982.1:g.4823C>G
NG_008982.2:g.4828C>G

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+313G>C
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