ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA15568334
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.29652100A>C
GRCh37
chr8:g.29509616A>C
Linked Data - Sequence & Population
gnomAD v2:
8:29509616 A / C
gnomAD v3:
8:29652100 A / C
gnomAD v4:
chr8-29652100-A-C
Joint Max Group AF
0.76247643 (SAS)
Genomes Max Group AF
0.76247643 (SAS)
Linked Data - NCBI & NCI
dbSNP:
9693444
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.29652100A>C , CM000670.2:g.29652100A>C
GRCh38
NC_000008.10:g.29509616A>C , CM000670.1:g.29509616A>C
GRCh37
NC_000008.9:g.29565535A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'