ClinGen Allele Registry
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Canonical Allele Identifier:
CA309551654
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.54404500C>T
Linked Data - Sequence & Population
gnomAD v3:
19:54404500 C / T
gnomAD v4:
chr19-54404500-C-T
Joint Max Group AF
0.62384884 (SAS)
Genomes Max Group AF
0.62384884 (SAS)
Linked Data - NCBI & NCI
dbSNP:
11084337
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.54404500C>T , CM000681.2:g.54404500C>T
GRCh38
NC_000019.8:g.59607916C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'