Canonical Allele Identifier: CA2242998169
Gene: MIR22HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1715087T= , CM000679.2:g.1715087T= GRCh38
NC_000017.10:g.1618381T= , CM000679.1:g.1618381T= GRCh37
NC_000017.9:g.1565131T= NCBI36
NG_032811.1:g.3565T=

Transcript Alleles

HGVS Amino-acid change
NR_028502.1:n.143+1043A=
NR_028503.1:n.143+1043A=
NR_028504.1:n.144-634A=
NR_028505.1:n.143+1043A=