ClinGen Allele Registry
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Canonical Allele Identifier:
CA201047982
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.134614732A>G
GRCh37
chr9:g.137506578A>G
Linked Data - Sequence & Population
gnomAD v2:
9:137506578 A / G
gnomAD v3:
9:134614732 A / G
gnomAD v4:
chr9-134614732-A-G
Joint Max Group AF
0.16756565 (AFR)
Genomes Max Group AF
0.16756565 (AFR)
Linked Data - NCBI & NCI
dbSNP:
11103429
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.134614732A>G , CM000671.2:g.134614732A>G
GRCh38
NC_000009.11:g.137506578A>G , CM000671.1:g.137506578A>G
GRCh37
NC_000009.10:g.136646399A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'