ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA16123282
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.197326170A>G
GRCh37
chr2:g.198190894A>G
Linked Data - Sequence & Population
gnomAD v2:
2:198190894 A / G
gnomAD v3:
2:197326170 A / G
gnomAD v4:
chr2-197326170-A-G
Joint Max Group AF
0.45999271 (EAS)
Genomes Max Group AF
0.45999271 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1429412
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.197326170A>G , CM000664.2:g.197326170A>G
GRCh38
NC_000002.11:g.198190894A>G , CM000664.1:g.198190894A>G
GRCh37
NC_000002.10:g.197899139A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'