ClinGen Allele Registry
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Canonical Allele Identifier:
CA15140898
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr1:g.47559391C>A
GRCh37
chr1:g.48025063C>A
Linked Data - Sequence & Population
gnomAD v2:
1:48025063 C / A
gnomAD v3:
1:47559391 C / A
gnomAD v4:
chr1-47559391-C-A
Joint Max Group AF
0.93707691 (EAS)
Genomes Max Group AF
0.93707691 (EAS)
Linked Data - NCBI & NCI
dbSNP:
685001
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.47559391C>A , CM000663.2:g.47559391C>A
GRCh38
NC_000001.10:g.48025063C>A , CM000663.1:g.48025063C>A
GRCh37
NC_000001.9:g.47797650C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'