ClinGen Allele Registry
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Canonical Allele Identifier:
CA23486202
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr1:g.67307127C>T
GRCh37
chr1:g.67772810C>T
Linked Data - Sequence & Population
gnomAD v2:
1:67772810 C / T
gnomAD v3:
1:67307127 C / T
gnomAD v4:
chr1-67307127-C-T
Joint Max Group AF
0.16908498 (AFR)
Genomes Max Group AF
0.16908498 (AFR)
Linked Data - NCBI & NCI
dbSNP:
11810249
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.67307127C>T , CM000663.2:g.67307127C>T
GRCh38
NC_000001.10:g.67772810C>T , CM000663.1:g.67772810C>T
GRCh37
NC_000001.9:g.67545398C>T
NCBI36
NG_032977.1:g.4764C>T
NG_032977.2:g.4777C>T
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