Canonical Allele Identifier: CA1081639573
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1751415991

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350502A>G , CM000667.2:g.132350502A>G GRCh38
NC_000005.9:g.131686195A>G , CM000667.1:g.131686195A>G GRCh37
NC_000005.8:g.131714094A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.418-545T>C