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Canonical Allele Identifier:
CA16292611
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr7:g.15024208T>G
GRCh37
chr7:g.15063833T>G
Linked Data - Sequence & Population
gnomAD v2:
7:15063833 T / G
gnomAD v3:
7:15024208 T / G
gnomAD v4:
chr7-15024208-T-G
Joint Max Group AF
0.66198105 (EAS)
Genomes Max Group AF
0.66198105 (EAS)
Linked Data - NCBI & NCI
dbSNP:
10244051
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.15024208T>G , CM000669.2:g.15024208T>G
GRCh38
NC_000007.13:g.15063833T>G , CM000669.1:g.15063833T>G
GRCh37
NC_000007.12:g.15030358T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'