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Canonical Allele Identifier:
CA78687665
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr3:g.84431917G>T
GRCh37
chr3:g.84481068G>T
Linked Data - Sequence & Population
gnomAD v2:
3:84481068 G / T
gnomAD v3:
3:84431917 G / T
gnomAD v4:
chr3-84431917-G-T
Joint Max Group AF
0.18326455 (EAS)
Genomes Max Group AF
0.18326455 (EAS)
Linked Data - NCBI & NCI
dbSNP:
10511089
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.84431917G>T , CM000665.2:g.84431917G>T
GRCh38
NC_000003.11:g.84481068G>T , CM000665.1:g.84481068G>T
GRCh37
NC_000003.10:g.84563758G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'