ClinGen Allele Registry
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Canonical Allele Identifier:
CA12984201
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr9:g.27630564T>C
GRCh37
chr9:g.27630562T>C
Linked Data - Sequence & Population
gnomAD v2:
9:27630562 T / C
gnomAD v3:
9:27630564 T / C
gnomAD v4:
chr9-27630564-T-C
Joint Max Group AF
0.38353467 (MID)
Genomes Max Group AF
0.3714149 (NFE)
Linked Data - NCBI & NCI
dbSNP:
12555345
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.27630564T>C , CM000671.2:g.27630564T>C
GRCh38
NC_000009.11:g.27630562T>C , CM000671.1:g.27630562T>C
GRCh37
NC_000009.10:g.27620562T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'