Allele Registry

Canonical Allele Identifier: CA257183

Gene:

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chr9:g.35658028_35658042dupGCTTCACAGAGTAGT

GRCh38 chr9:g.35658027_35658028insGCTTCACAGAGTAGT

GRCh37 chr9:g.35658025_35658039dupGCTTCACAGAGTAGT

GRCh37 chr9:g.35658024_35658025insGCTTCACAGAGTAGT

Linked Data - Sequence & Population

gnomAD v2:

9:35658024 A / AGCTTCACAGAGTAGT

gnomAD v3:

9:35658027 A / AGCTTCACAGAGTAGT

gnomAD v4:

chr9-35658027-A-AGCTTCACAGAGTAGT

Joint Max Group AF 0.00032569 (NFE)

Genomes Max Group AF 0.00029242 (NFE)

Exomes Max Group AF 0.00031414 (NFE)

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000015279

RCV000694726

RCV002223757

RCV002496370

ClinVar Variation:

14211

dbSNP:

727502776

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658028_35658042dup , CM000671.2:g.35658028_35658042dup	GRCh38
NC_000009.11:g.35658025_35658039dup , CM000671.1:g.35658025_35658039dup	GRCh37
NC_000009.10:g.35648025_35648039dup	NCBI36
NG_017041.1:g.4977_4991dup , LRG_163:g.4977_4991dup
NG_033120.1:g.4739_4753dup

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