Canonical Allele Identifier: CA192745806
Gene:

Linked Data

ClinVar Variation Id: 970375
ClinVar RCV Id: RCV001245938
dbSNP Id: rs553651882
gnomAD v2: 9-35658092-G-A
gnomAD v3: 9-35658095-G-A
gnomAD v4: 9-35658095-G-A
MyVariant Identifiers: chr9:g.35658092G>A (hg19) chr9:g.35658095G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35658095G>A , CM000671.2:g.35658095G>A GRCh38
NC_000009.11:g.35658092G>A , CM000671.1:g.35658092G>A GRCh37
NC_000009.10:g.35648092G>A NCBI36
NG_017041.1:g.4924C>T , LRG_163:g.4924C>T
NG_033120.1:g.4806G>A
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