ClinGen Allele Registry
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Canonical Allele Identifier:
CA15626457
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.99870872A>G
GRCh37
chr9:g.102633154A>G
Linked Data - Sequence & Population
gnomAD v2:
9:102633154 A / G
gnomAD v3:
9:99870872 A / G
gnomAD v4:
chr9-99870872-A-G
Joint Max Group AF
0.68538058 (NFE)
Genomes Max Group AF
0.68538058 (NFE)
Linked Data - NCBI & NCI
dbSNP:
10819699
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.99870872A>G , CM000671.2:g.99870872A>G
GRCh38
NC_000009.11:g.102633154A>G , CM000671.1:g.102633154A>G
GRCh37
NC_000009.10:g.101672975A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'