Canonical Allele Identifier: CA1583129118
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1751414165

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350325C>A , CM000667.2:g.132350325C>A GRCh38
NC_000005.9:g.131686018C>A , CM000667.1:g.131686018C>A GRCh37
NC_000005.8:g.131713917C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110997.1:n.418-368G>T