ClinGen Allele Registry
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Canonical Allele Identifier:
CA223486736
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.69211113G>A
GRCh37
chr11:g.68978580G>A
Linked Data - Sequence & Population
gnomAD v2:
11:68978580 G / A
gnomAD v3:
11:69211113 G / A
gnomAD v4:
chr11-69211113-G-A
Joint Max Group AF
0.24263783 (MID)
Genomes Max Group AF
0.20733148 (NFE)
Linked Data - NCBI & NCI
dbSNP:
11228565
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.69211113G>A , CM000673.2:g.69211113G>A
GRCh38
NC_000011.9:g.68978580G>A , CM000673.1:g.68978580G>A
GRCh37
NC_000011.8:g.68735156G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'