Canonical Allele Identifier: CA1583137359
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1751796025

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369633del , CM000667.2:g.132369633del GRCh38
NC_000005.9:g.131705325del , CM000667.1:g.131705325del GRCh37
NC_000005.8:g.131733224del NCBI36
NG_008982.1:g.4925del
NG_008982.2:g.4930del

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+212del