ClinGen Allele Registry
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Canonical Allele Identifier:
CA11032469
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.143898268A>G
GRCh37
chr2:g.144655836A>G
Linked Data - Sequence & Population
gnomAD v2:
2:144655836 A / G
gnomAD v3:
2:143898268 A / G
gnomAD v4:
chr2-143898268-A-G
Joint Max Group AF
0.94354868 (EAS)
Genomes Max Group AF
0.94354868 (EAS)
Linked Data - NCBI & NCI
dbSNP:
787151
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.143898268A>G , CM000664.2:g.143898268A>G
GRCh38
NC_000002.11:g.144655836A>G , CM000664.1:g.144655836A>G
GRCh37
NC_000002.10:g.144372306A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'