ClinGen Allele Registry
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Canonical Allele Identifier:
CA11509483
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.119569567A>C
GRCh37
chr3:g.119288414A>C
Linked Data - Sequence & Population
gnomAD v2:
3:119288414 A / C
gnomAD v3:
3:119569567 A / C
gnomAD v4:
chr3-119569567-A-C
Joint Max Group AF
0.26791471 (SAS)
Genomes Max Group AF
0.26791471 (SAS)
Linked Data - NCBI & NCI
dbSNP:
59374417
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.119569567A>C , CM000665.2:g.119569567A>C
GRCh38
NC_000003.11:g.119288414A>C , CM000665.1:g.119288414A>C
GRCh37
NC_000003.10:g.120771104A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'