ClinGen Allele Registry
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Canonical Allele Identifier:
CA134098328
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.11617934T>A
GRCh37
chr6:g.11618167T>A
Linked Data - Sequence & Population
gnomAD v2:
6:11618167 T / A
gnomAD v3:
6:11617934 T / A
gnomAD v4:
chr6-11617934-T-A
Joint Max Group AF
0.00001172 (NFE)
Genomes Max Group AF
0.00001172 (NFE)
Linked Data - NCBI & NCI
dbSNP:
479526
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.11617934T>A , CM000668.2:g.11617934T>A
GRCh38
NC_000006.11:g.11618167T>A , CM000668.1:g.11618167T>A
GRCh37
NC_000006.10:g.11726153T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'