Canonical Allele Identifier: CA2839561562
Gene: MIR22HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1715119A>T , CM000679.2:g.1715119A>T GRCh38
NC_000017.10:g.1618413A>T , CM000679.1:g.1618413A>T GRCh37
NC_000017.9:g.1565163A>T NCBI36
NG_032811.1:g.3597A>T

Transcript Alleles

HGVS Amino-acid Change
NR_028502.1:n.143+1011T>A
NR_028503.1:n.143+1011T>A
NR_028504.1:n.144-666T>A
NR_028505.1:n.143+1011T>A