Canonical Allele Identifier: CA2547341317
Gene: MIR22HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1715109T>C , CM000679.2:g.1715109T>C GRCh38
NC_000017.10:g.1618403T>C , CM000679.1:g.1618403T>C GRCh37
NC_000017.9:g.1565153T>C NCBI36
NG_032811.1:g.3587T>C

Transcript Alleles

HGVS Amino-acid change
NR_028502.1:n.143+1021A>G
NR_028503.1:n.143+1021A>G
NR_028504.1:n.144-656A>G
NR_028505.1:n.143+1021A>G