ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA11506258
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.96076432T>G
GRCh37
chr3:g.95795276T>G
Linked Data - Sequence & Population
gnomAD v2:
3:95795276 T / G
gnomAD v3:
3:96076432 T / G
gnomAD v4:
chr3-96076432-T-G
Joint Max Group AF
0.59916031 (AFR)
Genomes Max Group AF
0.59916031 (AFR)
Linked Data - NCBI & NCI
dbSNP:
4390941
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.96076432T>G , CM000665.2:g.96076432T>G
GRCh38
NC_000003.11:g.95795276T>G , CM000665.1:g.95795276T>G
GRCh37
NC_000003.10:g.97277966T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'