Canonical Allele Identifier: CA638742304
Gene:

Linked Data

ClinVar Variation Id: 1244768
ClinVar RCV Id: RCV001648976
dbSNP Id: rs1202324430
gnomAD v2: 22-25627898-TGA-T
gnomAD v3: 22-25231931-TGA-T
gnomAD v4: 22-25231931-TGA-T
MyVariant Identifiers: chr22:g.25627899_25627900del (hg19) chr22:g.25231932_25231933del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.25231955_25231956del , CM000684.2:g.25231955_25231956del GRCh38
NC_000022.10:g.25627922_25627923del , CM000684.1:g.25627922_25627923del GRCh37
NC_000022.9:g.23957922_23957923del NCBI36
NG_009827.1:g.17311_17312del
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