ClinGen Allele Registry
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Canonical Allele Identifier:
CA14926057
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr22:g.36215187T>C
GRCh37
chr22:g.36611233T>C
Linked Data - Sequence & Population
gnomAD v2:
22:36611233 T / C
gnomAD v3:
22:36215187 T / C
gnomAD v4:
chr22-36215187-T-C
Joint Max Group AF
0.32931709 (NFE)
Genomes Max Group AF
0.32931709 (NFE)
Linked Data - NCBI & NCI
dbSNP:
9610449
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.36215187T>C , CM000684.2:g.36215187T>C
GRCh38
NC_000022.10:g.36611233T>C , CM000684.1:g.36611233T>C
GRCh37
NC_000022.9:g.34941179T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'