Canonical Allele Identifier: CA1583129089
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1751413362

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350264G>A , CM000667.2:g.132350264G>A GRCh38
NC_000005.9:g.131685957G>A , CM000667.1:g.131685957G>A GRCh37
NC_000005.8:g.131713856G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.418-307C>T