ClinGen Allele Registry
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Canonical Allele Identifier:
CA703678973
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.106772332C>A
Linked Data - Sequence & Population
gnomAD v3:
14:106772332 C / A
gnomAD v4:
chr14-106772332-C-A
Linked Data - NCBI & NCI
dbSNP:
2337406
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.106772332C>A , CM000676.2:g.106772332C>A
GRCh38
Search 100 bp 5'
Search 100 bp 3'