ClinGen Allele Registry
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Canonical Allele Identifier:
CA12960630
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.84667612C>T
GRCh37
chr9:g.87282527C>T
Linked Data - Sequence & Population
gnomAD v2:
9:87282527 C / T
gnomAD v3:
9:84667612 C / T
gnomAD v4:
chr9-84667612-C-T
Joint Max Group AF
0.56845895 (NFE)
Genomes Max Group AF
0.56845895 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1212171
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.84667612C>T , CM000671.2:g.84667612C>T
GRCh38
NC_000009.11:g.87282527C>T , CM000671.1:g.87282527C>T
GRCh37
NC_000009.10:g.86472347C>T
NCBI36
NG_012201.2:g.4062C>T
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