ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA15705661
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr11:g.29173590A>G
GRCh37
chr11:g.29195137A>G
Linked Data - Sequence & Population
gnomAD v2:
11:29195137 A / G
gnomAD v3:
11:29173590 A / G
gnomAD v4:
chr11-29173590-A-G
Joint Max Group AF
0.39137007 (EAS)
Genomes Max Group AF
0.39137007 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1491818
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.29173590A>G , CM000673.2:g.29173590A>G
GRCh38
NC_000011.9:g.29195137A>G , CM000673.1:g.29195137A>G
GRCh37
NC_000011.8:g.29151713A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'