Canonical Allele Identifier: CA1583137363
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1751796312

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369640G>A , CM000667.2:g.132369640G>A GRCh38
NC_000005.9:g.131705332G>A , CM000667.1:g.131705332G>A GRCh37
NC_000005.8:g.131733231G>A NCBI36
NG_008982.1:g.4932G>A
NG_008982.2:g.4937G>A

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+204C>T