ClinGen Allele Registry
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Canonical Allele Identifier:
CA14063358
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.87829256A>G
GRCh37
chr14:g.88295600A>G
Linked Data - Sequence & Population
gnomAD v2:
14:88295600 A / G
gnomAD v3:
14:87829256 A / G
gnomAD v4:
chr14-87829256-A-G
Joint Max Group AF
0.92015695 (EAS)
Genomes Max Group AF
0.92015695 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4322600
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.87829256A>G , CM000676.2:g.87829256A>G
GRCh38
NC_000014.8:g.88295600A>G , CM000676.1:g.88295600A>G
GRCh37
NC_000014.7:g.87365353A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'