ClinGen Allele Registry
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Canonical Allele Identifier:
CA16599484
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr22:g.37110640T>C
GRCh37
chr22:g.37506680T>C
Linked Data - Sequence & Population
gnomAD v2:
22:37506680 T / C
gnomAD v3:
22:37110640 T / C
gnomAD v4:
chr22-37110640-T-C
Joint Max Group AF
0.47051487 (SAS)
Genomes Max Group AF
0.47051487 (SAS)
Linked Data - NCBI & NCI
dbSNP:
228918
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.37110640T>C , CM000684.2:g.37110640T>C
GRCh38
NC_000022.10:g.37506680T>C , CM000684.1:g.37506680T>C
GRCh37
NC_000022.9:g.35836626T>C
NCBI36
NG_012856.2:g.3924A>G
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