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Canonical Allele Identifier:
CA15676411
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.65481674A>G
GRCh37
chr11:g.65249145A>G
Linked Data - Sequence & Population
gnomAD v2:
11:65249145 A / G
gnomAD v3:
11:65481674 A / G
gnomAD v4:
chr11-65481674-A-G
Joint Max Group AF
0.2148188 (MID)
Genomes Max Group AF
0.19296331 (NFE)
Linked Data - NCBI & NCI
dbSNP:
17146964
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.65481674A>G , CM000673.2:g.65481674A>G
GRCh38
NC_000011.9:g.65249145A>G , CM000673.1:g.65249145A>G
GRCh37
NC_000011.8:g.65005721A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'