Canonical Allele Identifier: CA2768435795
Gene: MIR3936HG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369519A>T , CM000667.2:g.132369519A>T GRCh38
NC_000005.9:g.131705211A>T , CM000667.1:g.131705211A>T GRCh37
NC_000005.8:g.131733110A>T NCBI36
NG_008982.1:g.4811A>T
NG_008982.2:g.4816A>T

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+325T>A
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