ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA11457671
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr3:g.153004186C>T
GRCh37
chr3:g.152721975C>T
Linked Data - Sequence & Population
gnomAD v2:
3:152721975 C / T
gnomAD v3:
3:153004186 C / T
gnomAD v4:
chr3-153004186-C-T
Joint Max Group AF
0.58583634 (AFR)
Genomes Max Group AF
0.58583634 (AFR)
Linked Data - NCBI & NCI
dbSNP:
9883654
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.153004186C>T , CM000665.2:g.153004186C>T
GRCh38
NC_000003.11:g.152721975C>T , CM000665.1:g.152721975C>T
GRCh37
NC_000003.10:g.154204665C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'