Canonical Allele Identifier: CA286856289
Gene: MIR22HG HGNC NCBI

Linked Data

dbSNP Id: rs563774180
gnomAD v3: 17-1715212-C-G
gnomAD v4: 17-1715212-C-G
MyVariant Identifiers: chr17:g.1618506C>G (hg19) chr17:g.1715212C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1715212C>G , CM000679.2:g.1715212C>G GRCh38
NC_000017.10:g.1618506C>G , CM000679.1:g.1618506C>G GRCh37
NC_000017.9:g.1565256C>G NCBI36
NG_032811.1:g.3690C>G

Transcript Alleles

HGVS Amino-acid Change
NR_028502.1:n.143+918G>C
NR_028503.1:n.143+918G>C
NR_028504.1:n.144-759G>C
NR_028505.1:n.143+918G>C
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