ClinGen Allele Registry
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Canonical Allele Identifier:
CA15889042
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.58634662G>A
GRCh37
chr16:g.58668566G>A
Linked Data - Sequence & Population
gnomAD v2:
16:58668566 G / A
gnomAD v3:
16:58634662 G / A
gnomAD v4:
chr16-58634662-G-A
Joint Max Group AF
0.40392836 (NFE)
Genomes Max Group AF
0.40392836 (NFE)
Linked Data - NCBI & NCI
dbSNP:
149428
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.58634662G>A , CM000678.2:g.58634662G>A
GRCh38
NC_000016.9:g.58668566G>A , CM000678.1:g.58668566G>A
GRCh37
NC_000016.8:g.57226067G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'