ClinGen Allele Registry
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Canonical Allele Identifier:
CA13387840
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.72215616G>A
GRCh37
chr11:g.71926660G>A
Linked Data - Sequence & Population
gnomAD v2:
11:71926660 G / A
gnomAD v3:
11:72215616 G / A
gnomAD v4:
chr11-72215616-G-A
Joint Max Group AF
0.69523722 (AFR)
Genomes Max Group AF
0.69523722 (AFR)
Linked Data - NCBI & NCI
dbSNP:
651933
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.72215616G>A , CM000673.2:g.72215616G>A
GRCh38
NC_000011.9:g.71926660G>A , CM000673.1:g.71926660G>A
GRCh37
NC_000011.8:g.71604308G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'