ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA43945564
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.21174310G>A
GRCh37
chr2:g.21397182G>A
Linked Data - Sequence & Population
gnomAD v2:
2:21397182 G / A
gnomAD v3:
2:21174310 G / A
gnomAD v4:
chr2-21174310-G-A
Joint Max Group AF
0.97091736 (EAS)
Genomes Max Group AF
0.97091736 (EAS)
Linked Data - NCBI & NCI
dbSNP:
506585
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.21174310G>A , CM000664.2:g.21174310G>A
GRCh38
NC_000002.11:g.21397182G>A , CM000664.1:g.21397182G>A
GRCh37
NC_000002.10:g.21250687G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'