Canonical Allele Identifier: CA2580616181
Gene:

Linked Data

ClinVar Variation Id: 1696063
ClinVar RCV Id: RCV002266206 RCV003594177
dbSNP Id: rs727502778
gnomAD v4: 9-35658020-C-CGTCCTCAGCTTCACAGAGTCCTCAGCTTCACAGA
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35658039_35658040insCCTCAGCTTCACAGAGTCCTCAGCTTCACAGAGT , CM000671.2:g.35658039_35658040insCCTCAGCTTCACAGAGTCCTCAGCTTCACAGAGT GRCh38
NC_000009.11:g.35658036_35658037insCCTCAGCTTCACAGAGTCCTCAGCTTCACAGAGT , CM000671.1:g.35658036_35658037insCCTCAGCTTCACAGAGTCCTCAGCTTCACAGAGT GRCh37
NC_000009.10:g.35648036_35648037insCCTCAGCTTCACAGAGTCCTCAGCTTCACAGAGT NCBI36
NG_017041.1:g.4998_4999insTCTGTGAAGCTGAGGACTCTGTGAAGCTGAGGAC , LRG_163:g.4998_4999insTCTGTGAAGCTGAGGACTCTGTGAAGCTGAGGAC
NG_033120.1:g.4750_4751insCCTCAGCTTCACAGAGTCCTCAGCTTCACAGAGT
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