ClinGen Allele Registry
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Canonical Allele Identifier:
CA79063611
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr3:g.87476299C>A
GRCh37
chr3:g.87525449C>A
Linked Data - Sequence & Population
gnomAD v2:
3:87525449 C / A
gnomAD v3:
3:87476299 C / A
gnomAD v4:
chr3-87476299-C-A
Joint Max Group AF
0.34874872 (AFR)
Genomes Max Group AF
0.34874872 (AFR)
Linked Data - NCBI & NCI
dbSNP:
9883474
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.87476299C>A , CM000665.2:g.87476299C>A
GRCh38
NC_000003.11:g.87525449C>A , CM000665.1:g.87525449C>A
GRCh37
NC_000003.10:g.87608139C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'