ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA11331570
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.207643083C>T
GRCh37
chr2:g.208507807C>T
Linked Data - Sequence & Population
gnomAD v2:
2:208507807 C / T
gnomAD v3:
2:207643083 C / T
gnomAD v4:
chr2-207643083-C-T
Joint Max Group AF
0.59061891 (EAS)
Genomes Max Group AF
0.59061891 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4675690
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.207643083C>T , CM000664.2:g.207643083C>T
GRCh38
NC_000002.11:g.208507807C>T , CM000664.1:g.208507807C>T
GRCh37
NC_000002.10:g.208216052C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'