ClinGen Allele Registry
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Canonical Allele Identifier:
CA14926836
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr22:g.37523260G>A
GRCh37
chr22:g.37919267G>A
Linked Data - Sequence & Population
gnomAD v2:
22:37919267 G / A
gnomAD v3:
22:37523260 G / A
gnomAD v4:
chr22-37523260-G-A
Joint Max Group AF
0.23123861 (SAS)
Genomes Max Group AF
0.23123861 (SAS)
Linked Data - NCBI & NCI
dbSNP:
9607469
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.37523260G>A , CM000684.2:g.37523260G>A
GRCh38
NC_000022.10:g.37919267G>A , CM000684.1:g.37919267G>A
GRCh37
NC_000022.9:g.36249213G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'