ClinGen Allele Registry
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Canonical Allele Identifier:
CA13018858
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.114783386C>T
GRCh37
chr9:g.117545666C>T
Linked Data - Sequence & Population
gnomAD v2:
9:117545666 C / T
gnomAD v3:
9:114783386 C / T
gnomAD v4:
chr9-114783386-C-T
Joint Max Group AF
0.405946 (AFR)
Genomes Max Group AF
0.405946 (AFR)
Linked Data - NCBI & NCI
dbSNP:
6478106
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.114783386C>T , CM000671.2:g.114783386C>T
GRCh38
NC_000009.11:g.117545666C>T , CM000671.1:g.117545666C>T
GRCh37
NC_000009.10:g.116585487C>T
NCBI36
NG_011488.2:g.27743G>A
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