ClinGen Allele Registry
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Canonical Allele Identifier:
CA16140529
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.39404797A>G
GRCh37
chr3:g.39446288A>G
Linked Data - Sequence & Population
gnomAD v2:
3:39446288 A / G
gnomAD v3:
3:39404797 A / G
gnomAD v4:
chr3-39404797-A-G
Joint Max Group AF
0.31617954 (NFE)
Genomes Max Group AF
0.31617954 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2133579
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.39404797A>G , CM000665.2:g.39404797A>G
GRCh38
NC_000003.11:g.39446288A>G , CM000665.1:g.39446288A>G
GRCh37
NC_000003.10:g.39421292A>G
NCBI36
NG_033234.1:g.3085A>G
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