ClinGen Allele Registry
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Canonical Allele Identifier:
CA120238833
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr5:g.63955024T>G
GRCh37
chr5:g.63250851T>G
Linked Data - Sequence & Population
gnomAD v2:
5:63250851 T / G
gnomAD v3:
5:63955024 T / G
gnomAD v4:
chr5-63955024-T-G
Joint Max Group AF
0.60870393 (EAS)
Genomes Max Group AF
0.60870393 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1364043
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.63955024T>G , CM000667.2:g.63955024T>G
GRCh38
NC_000005.9:g.63250851T>G , CM000667.1:g.63250851T>G
GRCh37
NC_000005.8:g.63286607T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'