Canonical Allele Identifier: CA2675194724
Gene: MIR3936HG HGNC NCBI

Linked Data

gnomAD v4: 5-132369695-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369695T>C , CM000667.2:g.132369695T>C GRCh38
NC_000005.9:g.131705387T>C , CM000667.1:g.131705387T>C GRCh37
NC_000005.8:g.131733286T>C NCBI36
NG_008982.1:g.4987T>C
NG_008982.2:g.4992T>C

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+149A>G
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