ClinGen Allele Registry
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Canonical Allele Identifier:
CA13089652
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.114806766T>C
GRCh37
chr9:g.117569046T>C
Linked Data - Sequence & Population
gnomAD v2:
9:117569046 T / C
gnomAD v3:
9:114806766 T / C
gnomAD v4:
chr9-114806766-T-C
Joint Max Group AF
0.87757872 (AFR)
Genomes Max Group AF
0.87757872 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7848647
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.114806766T>C , CM000671.2:g.114806766T>C
GRCh38
NC_000009.11:g.117569046T>C , CM000671.1:g.117569046T>C
GRCh37
NC_000009.10:g.116608867T>C
NCBI36
NG_011488.2:g.4363A>G
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