ClinGen Allele Registry
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Canonical Allele Identifier:
CA13494955
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.128316987T>G
GRCh37
chr11:g.128186882T>G
Linked Data - Sequence & Population
gnomAD v2:
11:128186882 T / G
gnomAD v3:
11:128316987 T / G
gnomAD v4:
chr11-128316987-T-G
Joint Max Group AF
0.48755142 (NFE)
Genomes Max Group AF
0.48755142 (NFE)
Linked Data - NCBI & NCI
dbSNP:
10893845
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.128316987T>G , CM000673.2:g.128316987T>G
GRCh38
NC_000011.9:g.128186882T>G , CM000673.1:g.128186882T>G
GRCh37
NC_000011.8:g.127692092T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'