ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA13406327
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.2289922T>G
GRCh37
chr11:g.2311152T>G
Linked Data - Sequence & Population
gnomAD v2:
11:2311152 T / G
gnomAD v3:
11:2289922 T / G
gnomAD v4:
chr11-2289922-T-G
Joint Max Group AF
0.50726913 (NFE)
Genomes Max Group AF
0.50726913 (NFE)
Linked Data - NCBI & NCI
dbSNP:
7944004
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.2289922T>G , CM000673.2:g.2289922T>G
GRCh38
NC_000011.9:g.2311152T>G , CM000673.1:g.2311152T>G
GRCh37
NC_000011.8:g.2267728T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'