ClinGen Allele Registry
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Canonical Allele Identifier:
CA13018899
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.114935551A>G
GRCh37
chr9:g.117697831A>G
Linked Data - Sequence & Population
gnomAD v2:
9:117697831 A / G
gnomAD v3:
9:114935551 A / G
gnomAD v4:
chr9-114935551-A-G
Joint Max Group AF
0.43173895 (AMR)
Genomes Max Group AF
0.43173895 (AMR)
Linked Data - NCBI & NCI
dbSNP:
2181033
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.114935551A>G , CM000671.2:g.114935551A>G
GRCh38
NC_000009.11:g.117697831A>G , CM000671.1:g.117697831A>G
GRCh37
NC_000009.10:g.116737652A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'