ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA11579864
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.8209103A>C
GRCh37
chr3:g.8250790A>C
Linked Data - Sequence & Population
gnomAD v2:
3:8250790 A / C
gnomAD v3:
3:8209103 A / C
gnomAD v4:
chr3-8209103-A-C
Joint Max Group AF
0.73783862 (EAS)
Genomes Max Group AF
0.73783862 (EAS)
Linked Data - NCBI & NCI
dbSNP:
9866825
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.8209103A>C , CM000665.2:g.8209103A>C
GRCh38
NC_000003.11:g.8250790A>C , CM000665.1:g.8250790A>C
GRCh37
NC_000003.10:g.8225790A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'