ClinGen Allele Registry
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Canonical Allele Identifier:
CA290294545
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.37746322G>A
Linked Data - Sequence & Population
gnomAD v3:
17:37746322 G / A
gnomAD v4:
chr17-37746322-G-A
Joint Max Group AF
0.00009048 (NFE)
Genomes Max Group AF
0.00009048 (NFE)
Linked Data - NCBI & NCI
dbSNP:
3760511
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.37746322G>A , CM000679.2:g.37746322G>A
GRCh38
NG_013019.2:g.3785C>T
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