Canonical Allele Identifier: CA192745808
Gene:

Linked Data

ClinVar Variation Id: 1383153
ClinVar RCV Id: RCV001892390
dbSNP Id: rs777581273
gnomAD v2: 9-35658100-AT-A
gnomAD v3: 9-35658103-AT-A
gnomAD v4: 9-35658103-AT-A
MyVariant Identifiers: chr9:g.35658101del (hg19) chr9:g.35658104del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35658105del , CM000671.2:g.35658105del GRCh38
NC_000009.11:g.35658102del , CM000671.1:g.35658102del GRCh37
NC_000009.10:g.35648102del NCBI36
NG_017041.1:g.4915del , LRG_163:g.4915del
NG_033120.1:g.4816del
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