ClinGen Allele Registry
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Canonical Allele Identifier:
CA15686885
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.67586935C>A
GRCh37
chr11:g.67354406C>A
Linked Data - Sequence & Population
gnomAD v2:
11:67354406 C / A
gnomAD v3:
11:67586935 C / A
gnomAD v4:
chr11-67586935-C-A
Joint Max Group AF
0.34342323 (NFE)
Genomes Max Group AF
0.34342323 (NFE)
Linked Data - NCBI & NCI
dbSNP:
947895
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.67586935C>A , CM000673.2:g.67586935C>A
GRCh38
NC_000011.9:g.67354406C>A , CM000673.1:g.67354406C>A
GRCh37
NC_000011.8:g.67110982C>A
NCBI36
NG_012075.1:g.8341C>A , LRG_723:g.8341C>A
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