ClinGen Allele Registry
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Canonical Allele Identifier:
CA10689360
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr1:g.162060117A>T
GRCh37
chr1:g.162029907A>T
Linked Data - Sequence & Population
gnomAD v2:
1:162029907 A / T
gnomAD v3:
1:162060117 A / T
gnomAD v4:
chr1-162060117-A-T
Joint Max Group AF
0.65156278 (NFE)
Genomes Max Group AF
0.65156278 (NFE)
Linked Data - NCBI & NCI
dbSNP:
4657139
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.162060117A>T , CM000663.2:g.162060117A>T
GRCh38
NC_000001.10:g.162029907A>T , CM000663.1:g.162029907A>T
GRCh37
NC_000001.9:g.160296531A>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'