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Canonical Allele Identifier:
CA300530118
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.51878594T>G
GRCh37
chr18:g.49404964T>G
Linked Data - Sequence & Population
gnomAD v2:
18:49404964 T / G
gnomAD v3:
18:51878594 T / G
gnomAD v4:
chr18-51878594-T-G
Joint Max Group AF
0.9877333 (NFE)
Genomes Max Group AF
0.9877333 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1351435
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.51878594T>G , CM000680.2:g.51878594T>G
GRCh38
NC_000018.9:g.49404964T>G , CM000680.1:g.49404964T>G
GRCh37
NC_000018.8:g.47658962T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'