Canonical Allele Identifier: CA16598406
Gene:

Linked Data

ClinVar Variation Id: 1238443
ClinVar RCV Id: RCV001638846
dbSNP Id: rs3761435
gnomAD v2: 22-32870574-A-G
gnomAD v3: 22-32474587-A-G
gnomAD v4: 22-32474587-A-G
MyVariant Identifiers: chr22:g.32870574A>G (hg19) chr22:g.32474587A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474587A>G , CM000684.2:g.32474587A>G GRCh38
NC_000022.10:g.32870574A>G , CM000684.1:g.32870574A>G GRCh37
NC_000022.9:g.31200574A>G NCBI36
NG_016001.1:g.4868A>G
NG_016001.2:g.4868A>G
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