ClinGen Allele Registry
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Canonical Allele Identifier:
CA224764229
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.73152652A>G
GRCh37
chr11:g.72863697A>G
Linked Data - Sequence & Population
gnomAD v2:
11:72863697 A / G
gnomAD v3:
11:73152652 A / G
gnomAD v4:
chr11-73152652-A-G
Joint Max Group AF
0.09410956 (EAS)
Genomes Max Group AF
0.09410956 (EAS)
Linked Data - NCBI & NCI
dbSNP:
11235667
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.73152652A>G , CM000673.2:g.73152652A>G
GRCh38
NC_000011.9:g.72863697A>G , CM000673.1:g.72863697A>G
GRCh37
NC_000011.8:g.72541345A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'