Canonical Allele Identifier: CA1254843448
Gene: MIR4432HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.60381637C= , CM000664.2:g.60381637C= GRCh38
NC_000002.11:g.60608772C= , CM000664.1:g.60608772C= GRCh37
NC_000002.10:g.60462276C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_132991.1:n.93+1307G=
NR_132992.1:n.70+9669G=