ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA11269563
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.20983311T>G
GRCh37
chr2:g.21206183T>G
Linked Data - Sequence & Population
gnomAD v2:
2:21206183 T / G
gnomAD v3:
2:20983311 T / G
gnomAD v4:
chr2-20983311-T-G
Joint Max Group AF
0.69235496 (EAS)
Genomes Max Group AF
0.69235496 (EAS)
Linked Data - NCBI & NCI
dbSNP:
6754295
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.20983311T>G , CM000664.2:g.20983311T>G
GRCh38
NC_000002.11:g.21206183T>G , CM000664.1:g.21206183T>G
GRCh37
Search 100 bp 5'
Search 100 bp 3'