ClinGen Allele Registry
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Canonical Allele Identifier:
CA10779969
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.118341350G>A
GRCh37
chr1:g.118883973G>A
Linked Data - Sequence & Population
gnomAD v2:
1:118883973 G / A
gnomAD v3:
1:118341350 G / A
gnomAD v4:
chr1-118341350-G-A
Joint Max Group AF
0.28631462 (SAS)
Genomes Max Group AF
0.28631462 (SAS)
Linked Data - NCBI & NCI
dbSNP:
12735613
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.118341350G>A , CM000663.2:g.118341350G>A
GRCh38
NC_000001.10:g.118883973G>A , CM000663.1:g.118883973G>A
GRCh37
NC_000001.9:g.118685496G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'