ClinGen Allele Registry
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Canonical Allele Identifier:
CA46568619
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr2:g.41777857A>G
GRCh37
chr2:g.42004997A>G
Linked Data - Sequence & Population
gnomAD v2:
2:42004997 A / G
gnomAD v3:
2:41777857 A / G
gnomAD v4:
chr2-41777857-A-G
Joint Max Group AF
0.20959288 (SAS)
Genomes Max Group AF
0.20959288 (SAS)
Linked Data - NCBI & NCI
dbSNP:
719593
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.41777857A>G , CM000664.2:g.41777857A>G
GRCh38
NC_000002.11:g.42004997A>G , CM000664.1:g.42004997A>G
GRCh37
NC_000002.10:g.41858501A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'