Canonical Allele Identifier: CA1583137352
Gene: MIR3936HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369623G= , CM000667.2:g.132369623G= GRCh38
NC_000005.9:g.131705315G= , CM000667.1:g.131705315G= GRCh37
NC_000005.8:g.131733214G= NCBI36
NG_008982.1:g.4915G=
NG_008982.2:g.4920G=

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+221C=