Canonical Allele Identifier: CA286856154
Gene: MIR22HG HGNC NCBI

Linked Data

dbSNP Id: rs933310990
MyVariant Identifiers: chr17:g.1618389C>T (hg19) chr17:g.1715095C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1715095C>T , CM000679.2:g.1715095C>T GRCh38
NC_000017.10:g.1618389C>T , CM000679.1:g.1618389C>T GRCh37
NC_000017.9:g.1565139C>T NCBI36
NG_032811.1:g.3573C>T

Transcript Alleles

HGVS Amino-acid change
NR_028502.1:n.143+1035G>A
NR_028503.1:n.143+1035G>A
NR_028504.1:n.144-642G>A
NR_028505.1:n.143+1035G>A
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