ClinGen Allele Registry
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Canonical Allele Identifier:
CA14941681
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr22:g.40646087A>C
GRCh37
chr22:g.41042091A>C
Linked Data - Sequence & Population
gnomAD v2:
22:41042091 A / C
gnomAD v3:
22:40646087 A / C
gnomAD v4:
chr22-40646087-A-C
Joint Max Group AF
0.34243784 (EAS)
Genomes Max Group AF
0.34243784 (EAS)
Linked Data - NCBI & NCI
dbSNP:
12159200
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.40646087A>C , CM000684.2:g.40646087A>C
GRCh38
NC_000022.10:g.41042091A>C , CM000684.1:g.41042091A>C
GRCh37
NC_000022.9:g.39372037A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'