Canonical Allele Identifier: CA192745787
Gene:

Linked Data

ClinVar Variation Id: 2918424
ClinVar RCV Id: RCV003761135
dbSNP Id: rs1030974270
gnomAD v2: 9-35658055-A-G
gnomAD v3: 9-35658058-A-G
gnomAD v4: 9-35658058-A-G
MyVariant Identifiers: chr9:g.35658055A>G (hg19) chr9:g.35658058A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35658058A>G , CM000671.2:g.35658058A>G GRCh38
NC_000009.11:g.35658055A>G , CM000671.1:g.35658055A>G GRCh37
NC_000009.10:g.35648055A>G NCBI36
NG_017041.1:g.4961T>C , LRG_163:g.4961T>C
NG_033120.1:g.4769A>G
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