Canonical Allele Identifier: CA726559040
Gene: MIR22HG HGNC NCBI

Linked Data

dbSNP Id: rs1398758935
gnomAD v3: 17-1715118-G-A
gnomAD v4: 17-1715118-G-A
MyVariant Identifiers: chr17:g.1618412G>A (hg19) chr17:g.1715118G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1715118G>A , CM000679.2:g.1715118G>A GRCh38
NC_000017.10:g.1618412G>A , CM000679.1:g.1618412G>A GRCh37
NC_000017.9:g.1565162G>A NCBI36
NG_032811.1:g.3596G>A

Transcript Alleles

HGVS Amino-acid change
NR_028502.1:n.143+1012C>T
NR_028503.1:n.143+1012C>T
NR_028504.1:n.144-665C>T
NR_028505.1:n.143+1012C>T
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