ClinGen Allele Registry
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Canonical Allele Identifier:
CA13012421
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr9:g.72272787A>C
GRCh37
chr9:g.74887703A>C
Linked Data - Sequence & Population
gnomAD v2:
9:74887703 A / C
gnomAD v3:
9:72272787 A / C
gnomAD v4:
chr9-72272787-A-C
Joint Max Group AF
0.32955381 (NFE)
Genomes Max Group AF
0.32955381 (NFE)
Linked Data - NCBI & NCI
dbSNP:
11143230
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.72272787A>C , CM000671.2:g.72272787A>C
GRCh38
NC_000009.11:g.74887703A>C , CM000671.1:g.74887703A>C
GRCh37
NC_000009.10:g.74077523A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'