ClinGen Allele Registry
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Canonical Allele Identifier:
CA11798587
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr4:g.186264231A>T
GRCh37
chr4:g.187185385A>T
Linked Data - Sequence & Population
gnomAD v2:
4:187185385 A / T
gnomAD v3:
4:186264231 A / T
gnomAD v4:
chr4-186264231-A-T
Joint Max Group AF
0.39747229 (NFE)
Genomes Max Group AF
0.39747229 (NFE)
Linked Data - NCBI & NCI
dbSNP:
3756008
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.186264231A>T , CM000666.2:g.186264231A>T
GRCh38
NC_000004.11:g.187185385A>T , CM000666.1:g.187185385A>T
GRCh37
NC_000004.10:g.187422379A>T
NCBI36
NG_008051.1:g.3268A>T , LRG_583:g.3268A>T
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