Canonical Allele Identifier: CA2675194719
Gene: MIR3936HG HGNC NCBI

Linked Data

gnomAD v4: 5-132369692-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369692G>A , CM000667.2:g.132369692G>A GRCh38
NC_000005.9:g.131705384G>A , CM000667.1:g.131705384G>A GRCh37
NC_000005.8:g.131733283G>A NCBI36
NG_008982.1:g.4984G>A
NG_008982.2:g.4989G>A

Transcript Alleles

HGVS Amino-acid change
NR_110997.1:n.73+152C>T
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