ClinGen Allele Registry
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Canonical Allele Identifier:
CA14926537
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr22:g.37110836A>G
GRCh37
chr22:g.37506876A>G
Linked Data - Sequence & Population
gnomAD v2:
22:37506876 A / G
gnomAD v3:
22:37110836 A / G
gnomAD v4:
chr22-37110836-A-G
Joint Max Group AF
0.46885548 (SAS)
Genomes Max Group AF
0.46885548 (SAS)
Linked Data - NCBI & NCI
dbSNP:
228921
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.37110836A>G , CM000684.2:g.37110836A>G
GRCh38
NC_000022.10:g.37506876A>G , CM000684.1:g.37506876A>G
GRCh37
NC_000022.9:g.35836822A>G
NCBI36
NG_012856.2:g.3728T>C
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