Canonical Allele Identifier: CA127211589
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs10058074

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350453G>A , CM000667.2:g.132350453G>A GRCh38
NC_000005.9:g.131686146G>A , CM000667.1:g.131686146G>A GRCh37
NC_000005.8:g.131714045G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110997.1:n.418-496C>T