ClinGen Allele Registry
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Canonical Allele Identifier:
CA13831294
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.52920559G>A
GRCh37
chr13:g.53494694G>A
Linked Data - Sequence & Population
gnomAD v2:
13:53494694 G / A
gnomAD v3:
13:52920559 G / A
gnomAD v4:
chr13-52920559-G-A
Joint Max Group AF
0.82253256 (NFE)
Genomes Max Group AF
0.82253256 (NFE)
Linked Data - NCBI & NCI
dbSNP:
9536318
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.52920559G>A , CM000675.2:g.52920559G>A
GRCh38
NC_000013.10:g.53494694G>A , CM000675.1:g.53494694G>A
GRCh37
NC_000013.9:g.52392695G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'