ClinGen Allele Registry
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Canonical Allele Identifier:
CA13487352
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr11:g.76570549C>T
GRCh37
chr11:g.76281593C>T
Linked Data - Sequence & Population
gnomAD v2:
11:76281593 C / T
gnomAD v3:
11:76570549 C / T
gnomAD v4:
chr11-76570549-C-T
Joint Max Group AF
0.44234371 (NFE)
Genomes Max Group AF
0.44234371 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2212434
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.76570549C>T , CM000673.2:g.76570549C>T
GRCh38
NC_000011.9:g.76281593C>T , CM000673.1:g.76281593C>T
GRCh37
NC_000011.8:g.75959241C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'