ClinGen Allele Registry
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Canonical Allele Identifier:
CA15680784
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.126158822T>C
GRCh37
chr11:g.126028717T>C
Linked Data - Sequence & Population
gnomAD v2:
11:126028717 T / C
gnomAD v3:
11:126158822 T / C
gnomAD v4:
chr11-126158822-T-C
Joint Max Group AF
0.66212173 (AFR)
Genomes Max Group AF
0.66212173 (AFR)
Linked Data - NCBI & NCI
dbSNP:
563519
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.126158822T>C , CM000673.2:g.126158822T>C
GRCh38
NC_000011.9:g.126028717T>C , CM000673.1:g.126028717T>C
GRCh37
NC_000011.8:g.125533927T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'