ClinGen Allele Registry
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Canonical Allele Identifier:
CA13908892
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr13:g.21241730G>A
GRCh37
chr13:g.21815869G>A
Linked Data - Sequence & Population
gnomAD v2:
13:21815869 G / A
gnomAD v3:
13:21241730 G / A
gnomAD v4:
chr13-21241730-G-A
Joint Max Group AF
0.22230168 (AFR)
Genomes Max Group AF
0.22230168 (AFR)
Linked Data - NCBI & NCI
dbSNP:
17064136
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.21241730G>A , CM000675.2:g.21241730G>A
GRCh38
NC_000013.10:g.21815869G>A , CM000675.1:g.21815869G>A
GRCh37
NC_000013.9:g.20713869G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'