Canonical Allele Identifier: CA192745799
Gene:

Linked Data

ClinVar Variation Id: 964928
ClinVar RCV Id: RCV001239255
dbSNP Id: rs3829077
gnomAD v2: 9-35658072-A-T
gnomAD v3: 9-35658075-A-T
gnomAD v4: 9-35658075-A-T
MyVariant Identifiers: chr9:g.35658072A>T (hg19) chr9:g.35658075A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35658075A>T , CM000671.2:g.35658075A>T GRCh38
NC_000009.11:g.35658072A>T , CM000671.1:g.35658072A>T GRCh37
NC_000009.10:g.35648072A>T NCBI36
NG_017041.1:g.4944T>A , LRG_163:g.4944T>A
NG_033120.1:g.4786A>T
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