ClinGen Allele Registry
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Canonical Allele Identifier:
CA13481777
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.35232539T>A
GRCh37
chr11:g.35254086T>A
Linked Data - Sequence & Population
gnomAD v2:
11:35254086 T / A
gnomAD v3:
11:35232539 T / A
gnomAD v4:
chr11-35232539-T-A
Joint Max Group AF
0.54353946 (SAS)
Genomes Max Group AF
0.54353946 (SAS)
Linked Data - NCBI & NCI
dbSNP:
4755392
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.35232539T>A , CM000673.2:g.35232539T>A
GRCh38
NC_000011.9:g.35254086T>A , CM000673.1:g.35254086T>A
GRCh37
NC_000011.8:g.35210662T>A
NCBI36
NG_008937.1:g.98670T>A
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