ClinGen Allele Registry
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Canonical Allele Identifier:
CA16124719
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.207527254A>G
GRCh37
chr2:g.208391978A>G
Linked Data - Sequence & Population
gnomAD v2:
2:208391978 A / G
gnomAD v3:
2:207527254 A / G
gnomAD v4:
chr2-207527254-A-G
Joint Max Group AF
0.62018086 (EAS)
Genomes Max Group AF
0.62018086 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2253206
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.207527254A>G , CM000664.2:g.207527254A>G
GRCh38
NC_000002.11:g.208391978A>G , CM000664.1:g.208391978A>G
GRCh37
NC_000002.10:g.208100223A>G
NCBI36
NG_023299.1:g.2363A>G
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