Canonical Allele Identifier: CA915206417
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1561559607

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369544G>A , CM000667.2:g.132369544G>A GRCh38
NC_000005.9:g.131705236G>A , CM000667.1:g.131705236G>A GRCh37
NC_000005.8:g.131733135G>A NCBI36
NG_008982.1:g.4836G>A
NG_008982.2:g.4841G>A

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+300C>T