Canonical Allele Identifier: CA15373588
Gene: MIR3936HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132364175A>G , CM000667.2:g.132364175A>G GRCh38
NC_000005.9:g.131699867A>G , CM000667.1:g.131699867A>G GRCh37
NC_000005.8:g.131727766A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.380+760T>C