ClinGen Allele Registry
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Canonical Allele Identifier:
CA59860906
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr2:g.168913876A>C
GRCh37
chr2:g.169770386A>C
Linked Data - Sequence & Population
gnomAD v2:
2:169770386 A / C
gnomAD v3:
2:168913876 A / C
gnomAD v4:
chr2-168913876-A-C
Joint Max Group AF
0.29061077 (EAS)
Genomes Max Group AF
0.29061077 (EAS)
Linked Data - NCBI & NCI
dbSNP:
16856187
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.168913876A>C , CM000664.2:g.168913876A>C
GRCh38
NC_000002.11:g.169770386A>C , CM000664.1:g.169770386A>C
GRCh37
NC_000002.10:g.169478632A>C
NCBI36
NG_007374.2:g.122521T>G
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