ClinGen Allele Registry
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Canonical Allele Identifier:
CA123811
Gene:
Linked Data
ClinVar RCV:
RCV000015271
RCV000015272
RCV000015273
RCV000015274
RCV003974826
ClinVar Variation:
14207
dbSNP:
1024611
2151345376
2151345377
2151345381
gnomAD v2:
17:32579788 A / G
gnomAD v3:
17:34252769 A / G
gnomAD v4:
chr17-34252769-A-G
Joint Max Group AF
0.53923479 (EAS)
Genomes Max Group AF
0.53923479 (EAS)
MyVariant.info:
GRCh38
chr17:g.34252769A>G
GRCh37
chr17:g.32579788A>G
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.34252769A>G , CM000679.2:g.34252769A>G
GRCh38
NC_000017.10:g.32579788A>G , CM000679.1:g.32579788A>G
GRCh37
NC_000017.9:g.29603901A>G
NCBI36
NG_012123.1:g.2493A>G
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