Canonical Allele Identifier: CA1583129201
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1751416949

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350573A>G , CM000667.2:g.132350573A>G GRCh38
NC_000005.9:g.131686266A>G , CM000667.1:g.131686266A>G GRCh37
NC_000005.8:g.131714165A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.418-616T>C