ClinGen Allele Registry
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Canonical Allele Identifier:
CA15619704
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.99275688A>G
GRCh37
chr9:g.102037970A>G
Linked Data - Sequence & Population
gnomAD v2:
9:102037970 A / G
gnomAD v3:
9:99275688 A / G
gnomAD v4:
chr9-99275688-A-G
Joint Max Group AF
0.29831801 (SAS)
Genomes Max Group AF
0.29831801 (SAS)
Linked Data - NCBI & NCI
dbSNP:
10819643
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.99275688A>G , CM000671.2:g.99275688A>G
GRCh38
NC_000009.11:g.102037970A>G , CM000671.1:g.102037970A>G
GRCh37
NC_000009.10:g.101077791A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'