ClinGen Allele Registry
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Canonical Allele Identifier:
CA13420465
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr11:g.68678956C>T
GRCh37
chr11:g.68446424C>T
Linked Data - Sequence & Population
gnomAD v2:
11:68446424 C / T
gnomAD v3:
11:68678956 C / T
gnomAD v4:
chr11-68678956-C-T
Joint Max Group AF
0.87332741 (AFR)
Genomes Max Group AF
0.87332741 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2187331
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.68678956C>T , CM000673.2:g.68678956C>T
GRCh38
NC_000011.9:g.68446424C>T , CM000673.1:g.68446424C>T
GRCh37
NC_000011.8:g.68203000C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_001748281.1:n.231-1966G>A
Search 100 bp 5'
Search 100 bp 3'