Canonical Allele Identifier: CA2710221589
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs2126753554

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350432T>G , CM000667.2:g.132350432T>G GRCh38
NC_000005.9:g.131686125T>G , CM000667.1:g.131686125T>G GRCh37
NC_000005.8:g.131714024T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110997.1:n.418-475A>C