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Canonical Allele Identifier:
CA14551869
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.65331539T>G
GRCh37
chr18:g.62998775T>G
Linked Data - Sequence & Population
gnomAD v2:
18:62998775 T / G
gnomAD v3:
18:65331539 T / G
gnomAD v4:
chr18-65331539-T-G
Joint Max Group AF
0.40671645 (EAS)
Genomes Max Group AF
0.40671645 (EAS)
Linked Data - NCBI & NCI
dbSNP:
8083346
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.65331539T>G , CM000680.2:g.65331539T>G
GRCh38
NC_000018.9:g.62998775T>G , CM000680.1:g.62998775T>G
GRCh37
NC_000018.8:g.61149755T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'