ClinGen Allele Registry
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Canonical Allele Identifier:
CA275136171
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.88702008A>G
GRCh37
chr15:g.89245239A>G
Linked Data - Sequence & Population
gnomAD v3:
15:88702008 A / G
gnomAD v4:
chr15-88702008-A-G
Joint Max Group AF
0.00001172 (NFE)
Genomes Max Group AF
0.00001172 (NFE)
Linked Data - NCBI & NCI
dbSNP:
4932194
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.88702008A>G , CM000677.2:g.88702008A>G
GRCh38
NC_000015.9:g.89245239A>G , CM000677.1:g.89245239A>G
GRCh37
NC_000015.8:g.87046243A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'