Canonical Allele Identifier: CA1254843464
Gene: MIR4432HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.60381666T= , CM000664.2:g.60381666T= GRCh38
NC_000002.11:g.60608801T= , CM000664.1:g.60608801T= GRCh37
NC_000002.10:g.60462305T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_132991.1:n.93+1278A=
NR_132992.1:n.70+9640A=