Canonical Allele Identifier: CA192745800
Gene:

Linked Data

ClinVar Variation Id: 1053310
ClinVar RCV Id: RCV001361640
dbSNP Id: rs545125827
gnomAD v2: 9-35658073-T-G
gnomAD v3: 9-35658076-T-G
gnomAD v4: 9-35658076-T-G
MyVariant Identifiers: chr9:g.35658073T>G (hg19) chr9:g.35658076T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35658076T>G , CM000671.2:g.35658076T>G GRCh38
NC_000009.11:g.35658073T>G , CM000671.1:g.35658073T>G GRCh37
NC_000009.10:g.35648073T>G NCBI36
NG_017041.1:g.4943A>C , LRG_163:g.4943A>C
NG_033120.1:g.4787T>G
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