ClinGen Allele Registry
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Canonical Allele Identifier:
CA10907821
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.152286602A>G
GRCh37
chr1:g.152259078A>G
Linked Data - Sequence & Population
gnomAD v2:
1:152259078 A / G
gnomAD v3:
1:152286602 A / G
gnomAD v4:
chr1-152286602-A-G
Joint Max Group AF
0.55335657 (EAS)
Genomes Max Group AF
0.55335657 (EAS)
Linked Data - NCBI & NCI
dbSNP:
11204971
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.152286602A>G , CM000663.2:g.152286602A>G
GRCh38
NC_000001.10:g.152259078A>G , CM000663.1:g.152259078A>G
GRCh37
NC_000001.9:g.150525702A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'