Canonical Allele Identifier: CA1254843456

Gene: MIR4432HG

Linked Data

• dbSNP Id: rs1673984863
• gnomAD v3: 2-60381651-C-T
• gnomAD v4: 2-60381651-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.60381651C>T , CM000664.2:g.60381651C>T	GRCh38
NC_000002.11:g.60608786C>T , CM000664.1:g.60608786C>T	GRCh37
NC_000002.10:g.60462290C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_132991.1:n.93+1293G>A
NR_132992.1:n.70+9655G>A