ClinGen Allele Registry
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Canonical Allele Identifier:
CA12985173
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.33180364C>T
GRCh37
chr9:g.33180362C>T
Linked Data - Sequence & Population
gnomAD v2:
9:33180362 C / T
gnomAD v3:
9:33180364 C / T
gnomAD v4:
chr9-33180364-C-T
Joint Max Group AF
0.51418972 (EAS)
Genomes Max Group AF
0.51418972 (EAS)
Linked Data - NCBI & NCI
dbSNP:
10813960
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.33180364C>T , CM000671.2:g.33180364C>T
GRCh38
NC_000009.11:g.33180362C>T , CM000671.1:g.33180362C>T
GRCh37
NC_000009.10:g.33170362C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'