ClinGen Allele Registry
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Canonical Allele Identifier:
CA13108941
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.128111149A>G
GRCh37
chr9:g.130873428A>G
Linked Data - Sequence & Population
gnomAD v2:
9:130873428 A / G
gnomAD v3:
9:128111149 A / G
gnomAD v4:
chr9-128111149-A-G
Joint Max Group AF
0.82878512 (NFE)
Genomes Max Group AF
0.8287801 (NFE)
Exomes Max Group AF
0.17768 (NFE)
Linked Data - NCBI & NCI
dbSNP:
4837240
2129768737
2129768749
2129768761
2129768792
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.128111149A>G , CM000671.2:g.128111149A>G
GRCh38
NC_000009.11:g.130873428A>G , CM000671.1:g.130873428A>G
GRCh37
NC_000009.10:g.129913249A>G
NCBI36
NG_032871.1:g.47950A>G
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