Canonical Allele Identifier: CA2242998221
Gene: MIR22HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1715159C= , CM000679.2:g.1715159C= GRCh38
NC_000017.10:g.1618453C= , CM000679.1:g.1618453C= GRCh37
NC_000017.9:g.1565203C= NCBI36
NG_032811.1:g.3637C=

Transcript Alleles

HGVS Amino-acid Change
NR_028502.1:n.143+971G=
NR_028503.1:n.143+971G=
NR_028504.1:n.144-706G=
NR_028505.1:n.143+971G=