ClinGen Allele Registry
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Canonical Allele Identifier:
CA11051609
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.238788964T>C
GRCh37
chr2:g.239697605T>C
Linked Data - Sequence & Population
gnomAD v2:
2:239697605 T / C
gnomAD v3:
2:238788964 T / C
gnomAD v4:
chr2-238788964-T-C
Joint Max Group AF
0.51429676 (NFE)
Genomes Max Group AF
0.51429676 (NFE)
Linked Data - NCBI & NCI
dbSNP:
11683401
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.238788964T>C , CM000664.2:g.238788964T>C
GRCh38
NC_000002.11:g.239697605T>C , CM000664.1:g.239697605T>C
GRCh37
NC_000002.10:g.239362355T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'