ClinGen Allele Registry
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Canonical Allele Identifier:
CA116024653
Gene:
Linked Data - Expert Curation
COSMIC:
COSN14439146
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.25902267C>T
GRCh37
chr5:g.25902376C>T
Linked Data - Sequence & Population
gnomAD v2:
5:25902376 C / T
gnomAD v3:
5:25902267 C / T
gnomAD v4:
chr5-25902267-C-T
Joint Max Group AF
0.00032019 (AFR)
Genomes Max Group AF
0.00032019 (AFR)
Linked Data - NCBI & NCI
dbSNP:
867376485
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.25902267C>T , CM000667.2:g.25902267C>T
GRCh38
NC_000005.9:g.25902376C>T , CM000667.1:g.25902376C>T
GRCh37
NC_000005.8:g.25938133C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'