ClinGen Allele Registry
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Canonical Allele Identifier:
CA76956851
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.69574037G>A
GRCh37
chr3:g.69623188G>A
Linked Data - Sequence & Population
gnomAD v2:
3:69623188 G / A
gnomAD v3:
3:69574037 G / A
gnomAD v4:
chr3-69574037-G-A
Joint Max Group AF
0.04220009 (EAS)
Genomes Max Group AF
0.04220009 (EAS)
Linked Data - NCBI & NCI
dbSNP:
7647307
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.69574037G>A , CM000665.2:g.69574037G>A
GRCh38
NC_000003.11:g.69623188G>A , CM000665.1:g.69623188G>A
GRCh37
NC_000003.10:g.69705878G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'