ClinGen Allele Registry
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Canonical Allele Identifier:
CA194561528
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.75661759C>T
GRCh37
chr9:g.78276675C>T
Linked Data - Sequence & Population
gnomAD v2:
9:78276675 C / T
gnomAD v3:
9:75661759 C / T
gnomAD v4:
chr9-75661759-C-T
Joint Max Group AF
0.06864787 (NFE)
Genomes Max Group AF
0.06864787 (NFE)
Linked Data - NCBI & NCI
dbSNP:
10512049
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.75661759C>T , CM000671.2:g.75661759C>T
GRCh38
NC_000009.11:g.78276675C>T , CM000671.1:g.78276675C>T
GRCh37
NC_000009.10:g.77466495C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'