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Canonical Allele Identifier:
CA13429990
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.116736721C>T
GRCh37
chr11:g.116607437C>T
Linked Data - Sequence & Population
gnomAD v2:
11:116607437 C / T
gnomAD v3:
11:116736721 C / T
gnomAD v4:
chr11-116736721-C-T
Joint Max Group AF
0.97617167 (AFR)
Genomes Max Group AF
0.97617167 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1558861
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.116736721C>T , CM000673.2:g.116736721C>T
GRCh38
NC_000011.9:g.116607437C>T , CM000673.1:g.116607437C>T
GRCh37
NC_000011.8:g.116112647C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'