Canonical Allele Identifier: CA1583129114
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1034024365

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350314T>G , CM000667.2:g.132350314T>G GRCh38
NC_000005.9:g.131686007T>G , CM000667.1:g.131686007T>G GRCh37
NC_000005.8:g.131713906T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110997.1:n.418-357A>C