ClinGen Allele Registry
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Canonical Allele Identifier:
CA290294550
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.37746322G>T
Linked Data - Sequence & Population
gnomAD v3:
17:37746322 G / T
gnomAD v4:
chr17-37746322-G-T
Joint Max Group AF
0.80822531 (AFR)
Genomes Max Group AF
0.80822531 (AFR)
Linked Data - NCBI & NCI
dbSNP:
3760511
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.37746322G>T , CM000679.2:g.37746322G>T
GRCh38
NG_013019.2:g.3785C>A
Search 100 bp 5'
Search 100 bp 3'