ClinGen Allele Registry
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Canonical Allele Identifier:
CA14997323
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr22:g.41361643G>A
GRCh37
chr22:g.41757647G>A
Linked Data - Sequence & Population
gnomAD v2:
22:41757647 G / A
gnomAD v3:
22:41361643 G / A
gnomAD v4:
chr22-41361643-G-A
Joint Max Group AF
0.44880731 (AMR)
Genomes Max Group AF
0.44880731 (AMR)
Linked Data - NCBI & NCI
dbSNP:
4822024
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.41361643G>A , CM000684.2:g.41361643G>A
GRCh38
NC_000022.10:g.41757647G>A , CM000684.1:g.41757647G>A
GRCh37
NC_000022.9:g.40087593G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'