ClinGen Allele Registry
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Canonical Allele Identifier:
CA191847533
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr9:g.26614849C>T
GRCh37
chr9:g.26614847C>T
Linked Data - Sequence & Population
gnomAD v2:
9:26614847 C / T
gnomAD v3:
9:26614849 C / T
gnomAD v4:
chr9-26614849-C-T
Joint Max Group AF
0.43435991 (AFR)
Genomes Max Group AF
0.43435991 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10812428
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.26614849C>T , CM000671.2:g.26614849C>T
GRCh38
NC_000009.11:g.26614847C>T , CM000671.1:g.26614847C>T
GRCh37
NC_000009.10:g.26604847C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'