Canonical Allele Identifier: CA1081639561
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1561553624

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350423G>A , CM000667.2:g.132350423G>A GRCh38
NC_000005.9:g.131686116G>A , CM000667.1:g.131686116G>A GRCh37
NC_000005.8:g.131714015G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110997.1:n.418-466C>T