ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA89630049
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.186748463G>A
GRCh37
chr3:g.186466252G>A
Linked Data - Sequence & Population
gnomAD v2:
3:186466252 G / A
gnomAD v3:
3:186748463 G / A
gnomAD v4:
chr3-186748463-G-A
Joint Max Group AF
0.26896128 (EAS)
Genomes Max Group AF
0.26896128 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1656966
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.186748463G>A , CM000665.2:g.186748463G>A
GRCh38
NC_000003.11:g.186466252G>A , CM000665.1:g.186466252G>A
GRCh37
NC_000003.10:g.187948946G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'