ClinGen Allele Registry
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Canonical Allele Identifier:
CA265717178
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.92918108G>A
GRCh37
chr14:g.93384453G>A
Linked Data - Sequence & Population
gnomAD v2:
14:93384453 G / A
gnomAD v3:
14:92918108 G / A
gnomAD v4:
chr14-92918108-G-A
Joint Max Group AF
0.06427694 (NFE)
Genomes Max Group AF
0.06427694 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1316506
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.92918108G>A , CM000676.2:g.92918108G>A
GRCh38
NC_000014.8:g.93384453G>A , CM000676.1:g.93384453G>A
GRCh37
NC_000014.7:g.92454206G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'