ClinGen Allele Registry
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Canonical Allele Identifier:
CA250234631
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.53533217G>A
GRCh37
chr13:g.54107352G>A
Linked Data - Sequence & Population
gnomAD v2:
13:54107352 G / A
gnomAD v3:
13:53533217 G / A
gnomAD v4:
chr13-53533217-G-A
Joint Max Group AF
0.27078544 (AMR)
Genomes Max Group AF
0.27078544 (AMR)
Linked Data - NCBI & NCI
dbSNP:
9568867
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.53533217G>A , CM000675.2:g.53533217G>A
GRCh38
NC_000013.10:g.54107352G>A , CM000675.1:g.54107352G>A
GRCh37
NC_000013.9:g.53005353G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'