ClinGen Allele Registry
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Canonical Allele Identifier:
CA13089861
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.118268751A>G
GRCh37
chr9:g.121031029A>G
Linked Data - Sequence & Population
gnomAD v2:
9:121031029 A / G
gnomAD v3:
9:118268751 A / G
gnomAD v4:
chr9-118268751-A-G
Joint Max Group AF
0.26628147 (AMR)
Genomes Max Group AF
0.26628147 (AMR)
Linked Data - NCBI & NCI
dbSNP:
876347
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.118268751A>G , CM000671.2:g.118268751A>G
GRCh38
NC_000009.11:g.121031029A>G , CM000671.1:g.121031029A>G
GRCh37
NC_000009.10:g.120070850A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'