ClinGen Allele Registry
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Canonical Allele Identifier:
CA23300792
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr1:g.59239775A>C
GRCh37
chr1:g.59705447A>C
Linked Data - Sequence & Population
gnomAD v2:
1:59705447 A / C
gnomAD v3:
1:59239775 A / C
gnomAD v4:
chr1-59239775-A-C
Joint Max Group AF
0.84857157 (EAS)
Genomes Max Group AF
0.84857157 (EAS)
Linked Data - NCBI & NCI
dbSNP:
6587852
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.59239775A>C , CM000663.2:g.59239775A>C
GRCh38
NC_000001.10:g.59705447A>C , CM000663.1:g.59705447A>C
GRCh37
NC_000001.9:g.59478035A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'