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Canonical Allele Identifier:
CA779991346
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.49001731A>T
GRCh37
chr18:g.46528101A>T
Linked Data - Sequence & Population
gnomAD v3:
18:49001731 A / T
gnomAD v4:
chr18-49001731-A-T
Joint Max Group AF
0.00000488 (NFE)
Genomes Max Group AF
0.00000488 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1476684335
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.49001731A>T , CM000680.2:g.49001731A>T
GRCh38
NC_000018.9:g.46528101A>T , CM000680.1:g.46528101A>T
GRCh37
NC_000018.8:g.44782099A>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'