Canonical Allele Identifier: CA286856148
Gene: MIR22HG HGNC NCBI

Linked Data

dbSNP Id: rs762055391
gnomAD v2: 17-1618364-C-G
gnomAD v3: 17-1715070-C-G
gnomAD v4: 17-1715070-C-G
MyVariant Identifiers: chr17:g.1618364C>G (hg19) chr17:g.1715070C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1715070C>G , CM000679.2:g.1715070C>G GRCh38
NC_000017.10:g.1618364C>G , CM000679.1:g.1618364C>G GRCh37
NC_000017.9:g.1565114C>G NCBI36
NG_032811.1:g.3548C>G

Transcript Alleles

HGVS Amino-acid change
NR_028502.1:n.144-1056G>C
NR_028503.1:n.144-1056G>C
NR_028504.1:n.144-617G>C
NR_028505.1:n.144-1056G>C
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