ClinGen Allele Registry
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Canonical Allele Identifier:
CA155176930
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr7:g.22069841G>A
GRCh37
chr7:g.22109459G>A
Linked Data - Sequence & Population
gnomAD v2:
7:22109459 G / A
gnomAD v3:
7:22069841 G / A
gnomAD v4:
chr7-22069841-G-A
Joint Max Group AF
0.33093396 (EAS)
Genomes Max Group AF
0.33093396 (EAS)
Linked Data - NCBI & NCI
dbSNP:
10499559
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.22069841G>A , CM000669.2:g.22069841G>A
GRCh38
NC_000007.13:g.22109459G>A , CM000669.1:g.22109459G>A
GRCh37
NC_000007.12:g.22075984G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'