Canonical Allele Identifier: CA1583137338
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1751793543

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369598dup , CM000667.2:g.132369598dup GRCh38
NC_000005.9:g.131705290dup , CM000667.1:g.131705290dup GRCh37
NC_000005.8:g.131733189dup NCBI36
NG_008982.1:g.4890dup
NG_008982.2:g.4895dup

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+246dup