Canonical Allele Identifier: CA1081634991
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1751791432
gnomAD v3: 5-132369555-C-G
gnomAD v4: 5-132369555-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369555C>G , CM000667.2:g.132369555C>G GRCh38
NC_000005.9:g.131705247C>G , CM000667.1:g.131705247C>G GRCh37
NC_000005.8:g.131733146C>G NCBI36
NG_008982.1:g.4847C>G
NG_008982.2:g.4852C>G

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+289G>C
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