ClinGen Allele Registry
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Canonical Allele Identifier:
CA13430008
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr11:g.116792991G>A
GRCh37
chr11:g.116663707G>A
Linked Data - Sequence & Population
gnomAD v2:
11:116663707 G / A
gnomAD v3:
11:116792991 G / A
gnomAD v4:
chr11-116792991-G-A
Joint Max Group AF
0.92850992 (NFE)
Genomes Max Group AF
0.92850992 (NFE)
Linked Data - NCBI & NCI
dbSNP:
662799
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.116792991G>A , CM000673.2:g.116792991G>A
GRCh38
NC_000011.9:g.116663707G>A , CM000673.1:g.116663707G>A
GRCh37
NC_000011.8:g.116168917G>A
NCBI36
NG_015894.1:g.4430C>T
NG_015894.2:g.4430C>T
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