Canonical Allele Identifier: CA2675194467
Gene: MIR3936HG HGNC NCBI

Linked Data

gnomAD v4: 5-132369526-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369526T>G , CM000667.2:g.132369526T>G GRCh38
NC_000005.9:g.131705218T>G , CM000667.1:g.131705218T>G GRCh37
NC_000005.8:g.131733117T>G NCBI36
NG_008982.1:g.4818T>G
NG_008982.2:g.4823T>G

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+318A>C
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