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Canonical Allele Identifier:
CA15851774
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr15:g.45349027C>A
GRCh37
chr15:g.45641225C>A
Linked Data - Sequence & Population
gnomAD v2:
15:45641225 C / A
gnomAD v3:
15:45349027 C / A
gnomAD v4:
chr15-45349027-C-A
Joint Max Group AF
0.88638931 (EAS)
Genomes Max Group AF
0.88638931 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2453533
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.45349027C>A , CM000677.2:g.45349027C>A
GRCh38
NC_000015.9:g.45641225C>A , CM000677.1:g.45641225C>A
GRCh37
NC_000015.8:g.43428517C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'