ClinGen Allele Registry
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Canonical Allele Identifier:
CA597926351
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.27315157C>A
GRCh37
chr11:g.27336704C>A
Linked Data - Sequence & Population
gnomAD v2:
11:27336704 C / A
gnomAD v3:
11:27315157 C / A
gnomAD v4:
chr11-27315157-C-A
Joint Max Group AF
0.00001172 (NFE)
Genomes Max Group AF
0.00001172 (NFE)
Linked Data - NCBI & NCI
dbSNP:
10160456
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.27315157C>A , CM000673.2:g.27315157C>A
GRCh38
NC_000011.9:g.27336704C>A , CM000673.1:g.27336704C>A
GRCh37
NC_000011.8:g.27293280C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'