Canonical Allele Identifier: CA638742303
Gene:

Linked Data

ClinVar Variation Id: 1241294
ClinVar RCV Id: RCV001645039
dbSNP Id: rs1202324430
gnomAD v2: 22-25627898-T-TGA
gnomAD v3: 22-25231931-T-TGA
gnomAD v4: 22-25231931-T-TGA
MyVariant Identifiers: chr22:g.25627900_25627901insGA (hg19) chr22:g.25627898_25627899insGA (hg19) chr22:g.25231933_25231934insGA (hg38) chr22:g.25231931_25231932insGA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.25231955_25231956dup , CM000684.2:g.25231955_25231956dup GRCh38
NC_000022.10:g.25627922_25627923dup , CM000684.1:g.25627922_25627923dup GRCh37
NC_000022.9:g.23957922_23957923dup NCBI36
NG_009827.1:g.17311_17312dup
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