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Canonical Allele Identifier:
CA16000711
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr22:g.36137737C>T
GRCh37
chr22:g.36533785C>T
Linked Data - Sequence & Population
gnomAD v2:
22:36533785 C / T
gnomAD v3:
22:36137737 C / T
gnomAD v4:
chr22-36137737-C-T
Joint Max Group AF
0.39001508 (SAS)
Genomes Max Group AF
0.39001508 (SAS)
Linked Data - NCBI & NCI
dbSNP:
132617
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.36137737C>T , CM000684.2:g.36137737C>T
GRCh38
NC_000022.10:g.36533785C>T , CM000684.1:g.36533785C>T
GRCh37
NC_000022.9:g.34863731C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'