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Canonical Allele Identifier:
CA15686026
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.92968430T>C
GRCh37
chr11:g.92701596T>C
Linked Data - Sequence & Population
gnomAD v2:
11:92701596 T / C
gnomAD v3:
11:92968430 T / C
gnomAD v4:
chr11-92968430-T-C
Joint Max Group AF
0.68135167 (EAS)
Genomes Max Group AF
0.68135167 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4753426
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.92968430T>C , CM000673.2:g.92968430T>C
GRCh38
NC_000011.9:g.92701596T>C , CM000673.1:g.92701596T>C
GRCh37
NC_000011.8:g.92341244T>C
NCBI36
NG_028160.1:g.3808T>C
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