ClinGen Allele Registry
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Canonical Allele Identifier:
CA260056513
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.42934256C>T
GRCh37
chr14:g.43403459C>T
Linked Data - Sequence & Population
gnomAD v2:
14:43403459 C / T
gnomAD v3:
14:42934256 C / T
gnomAD v4:
chr14-42934256-C-T
Joint Max Group AF
0.36168296 (AMR)
Genomes Max Group AF
0.36168296 (AMR)
Linked Data - NCBI & NCI
dbSNP:
11157317
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.42934256C>T , CM000676.2:g.42934256C>T
GRCh38
NC_000014.8:g.43403459C>T , CM000676.1:g.43403459C>T
GRCh37
NC_000014.7:g.42473209C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'