Canonical Allele Identifier: CA286856149
Gene: MIR22HG HGNC NCBI

Linked Data

dbSNP Id: rs922043879
gnomAD v2: 17-1618375-C-T
gnomAD v3: 17-1715081-C-T
gnomAD v4: 17-1715081-C-T
MyVariant Identifiers: chr17:g.1618375C>T (hg19) chr17:g.1715081C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1715081C>T , CM000679.2:g.1715081C>T GRCh38
NC_000017.10:g.1618375C>T , CM000679.1:g.1618375C>T GRCh37
NC_000017.9:g.1565125C>T NCBI36
NG_032811.1:g.3559C>T

Transcript Alleles

HGVS Amino-acid change
NR_028502.1:n.143+1049G>A
NR_028503.1:n.143+1049G>A
NR_028504.1:n.144-628G>A
NR_028505.1:n.143+1049G>A
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