ClinGen Allele Registry
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Canonical Allele Identifier:
CA156198060
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.32454195T>G
GRCh37
chr7:g.32493807T>G
Linked Data - Sequence & Population
gnomAD v2:
7:32493807 T / G
gnomAD v3:
7:32454195 T / G
gnomAD v4:
chr7-32454195-T-G
Joint Max Group AF
0.58722767 (EAS)
Genomes Max Group AF
0.58722767 (EAS)
Linked Data - NCBI & NCI
dbSNP:
6949851
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.32454195T>G , CM000669.2:g.32454195T>G
GRCh38
NC_000007.13:g.32493807T>G , CM000669.1:g.32493807T>G
GRCh37
NC_000007.12:g.32460332T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'