Canonical Allele Identifier: CA2242998177

Gene: MIR22HG

Linked Data

• dbSNP Id: rs1288022381

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1715096T>G , CM000679.2:g.1715096T>G	GRCh38
NC_000017.10:g.1618390T>G , CM000679.1:g.1618390T>G	GRCh37
NC_000017.9:g.1565140T>G	NCBI36
NG_032811.1:g.3574T>G

Transcript Alleles

HGVS	Amino-acid change
NR_028502.1:n.143+1034A>C
NR_028503.1:n.143+1034A>C
NR_028504.1:n.144-643A>C
NR_028505.1:n.143+1034A>C