ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA14165009
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.90350436C>A
GRCh37
chr15:g.90893668C>A
Linked Data - Sequence & Population
gnomAD v2:
15:90893668 C / A
gnomAD v3:
15:90350436 C / A
gnomAD v4:
chr15-90350436-C-A
Joint Max Group AF
0.3927146 (AFR)
Genomes Max Group AF
0.3927146 (AFR)
Linked Data - NCBI & NCI
dbSNP:
6496667
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.90350436C>A , CM000677.2:g.90350436C>A
GRCh38
NC_000015.9:g.90893668C>A , CM000677.1:g.90893668C>A
GRCh37
NC_000015.8:g.88694672C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'