ClinGen Allele Registry
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Canonical Allele Identifier:
CA155148346
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.22092263T>C
GRCh37
chr7:g.22131881T>C
Linked Data - Sequence & Population
gnomAD v2:
7:22131881 T / C
gnomAD v3:
7:22092263 T / C
gnomAD v4:
chr7-22092263-T-C
Joint Max Group AF
0.23929919 (AFR)
Genomes Max Group AF
0.23929919 (AFR)
Linked Data - NCBI & NCI
dbSNP:
4722094
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.22092263T>C , CM000669.2:g.22092263T>C
GRCh38
NC_000007.13:g.22131881T>C , CM000669.1:g.22131881T>C
GRCh37
NC_000007.12:g.22098406T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'