Canonical Allele Identifier: CA2242998182

Gene: MIR22HG

Linked Data

• dbSNP Id: rs1914437530

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1715100A>G , CM000679.2:g.1715100A>G	GRCh38
NC_000017.10:g.1618394A>G , CM000679.1:g.1618394A>G	GRCh37
NC_000017.9:g.1565144A>G	NCBI36
NG_032811.1:g.3578A>G

Transcript Alleles

HGVS	Amino-acid change
NR_028502.1:n.143+1030T>C
NR_028503.1:n.143+1030T>C
NR_028504.1:n.144-647T>C
NR_028505.1:n.143+1030T>C