Canonical Allele Identifier: CA980689334
Gene: MIR22HG HGNC NCBI

Linked Data

dbSNP Id: rs975986521
gnomAD v3: 17-1715097-G-A
gnomAD v4: 17-1715097-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1715097G>A , CM000679.2:g.1715097G>A GRCh38
NC_000017.10:g.1618391G>A , CM000679.1:g.1618391G>A GRCh37
NC_000017.9:g.1565141G>A NCBI36
NG_032811.1:g.3575G>A

Transcript Alleles

HGVS Amino-acid change
NR_028502.1:n.143+1033C>T
NR_028503.1:n.143+1033C>T
NR_028504.1:n.144-644C>T
NR_028505.1:n.143+1033C>T
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