ClinGen Allele Registry
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Canonical Allele Identifier:
CA134681471
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.9450964T>A
GRCh37
chr6:g.9451197T>A
Linked Data - Sequence & Population
gnomAD v2:
6:9451197 T / A
gnomAD v3:
6:9450964 T / A
gnomAD v4:
chr6-9450964-T-A
Joint Max Group AF
0.35156155 (EAS)
Genomes Max Group AF
0.35156155 (EAS)
Linked Data - NCBI & NCI
dbSNP:
10484246
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.9450964T>A , CM000668.2:g.9450964T>A
GRCh38
NC_000006.11:g.9451197T>A , CM000668.1:g.9451197T>A
GRCh37
NC_000006.10:g.9559183T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'