ClinGen Allele Registry
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Canonical Allele Identifier:
CA15385402
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.151098757G>A
GRCh37
chr5:g.150478318G>A
Linked Data - Sequence & Population
gnomAD v2:
5:150478318 G / A
gnomAD v3:
5:151098757 G / A
gnomAD v4:
chr5-151098757-G-A
Joint Max Group AF
0.12943313 (SAS)
Genomes Max Group AF
0.12943313 (SAS)
Linked Data - NCBI & NCI
dbSNP:
17728338
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.151098757G>A , CM000667.2:g.151098757G>A
GRCh38
NC_000005.9:g.150478318G>A , CM000667.1:g.150478318G>A
GRCh37
NC_000005.8:g.150458511G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'