Canonical Allele Identifier: CA2675194712
Gene: MIR3936HG HGNC NCBI

Linked Data

gnomAD v4: 5-132369687-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369687C>T , CM000667.2:g.132369687C>T GRCh38
NC_000005.9:g.131705379C>T , CM000667.1:g.131705379C>T GRCh37
NC_000005.8:g.131733278C>T NCBI36
NG_008982.1:g.4979C>T
NG_008982.2:g.4984C>T

Transcript Alleles

HGVS Amino-acid change
NR_110997.1:n.73+157G>A
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