Canonical Allele Identifier: CA624478997
Gene: MIR22HG HGNC NCBI

Linked Data

dbSNP Id: rs1288022381
gnomAD v2: 17-1618390-T-C
gnomAD v3: 17-1715096-T-C
gnomAD v4: 17-1715096-T-C
MyVariant Identifiers: chr17:g.1618390T>C (hg19) chr17:g.1715096T>C (hg38)
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Genomic Alleles

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

Transcript Alleles

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