Canonical Allele Identifier: CA2242998168
Gene: MIR22HG HGNC NCBI

Linked Data

dbSNP Id: rs1914436315
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1715084C>A , CM000679.2:g.1715084C>A GRCh38
NC_000017.10:g.1618378C>A , CM000679.1:g.1618378C>A GRCh37
NC_000017.9:g.1565128C>A NCBI36
NG_032811.1:g.3562C>A

Transcript Alleles

HGVS Amino-acid change
NR_028502.1:n.143+1046G>T
NR_028503.1:n.143+1046G>T
NR_028504.1:n.144-631G>T
NR_028505.1:n.143+1046G>T
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