Canonical Allele Identifier: CA2242998183
Gene: MIR22HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1715101T= , CM000679.2:g.1715101T= GRCh38
NC_000017.10:g.1618395T= , CM000679.1:g.1618395T= GRCh37
NC_000017.9:g.1565145T= NCBI36
NG_032811.1:g.3579T=

Transcript Alleles

HGVS Amino-acid change
NR_028502.1:n.143+1029A=
NR_028503.1:n.143+1029A=
NR_028504.1:n.144-648A=
NR_028505.1:n.143+1029A=