ClinGen Allele Registry
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Canonical Allele Identifier:
CA707769193
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr14:g.65178532T>A
GRCh37
chr14:g.65645250T>A
Linked Data - Sequence & Population
gnomAD v3:
14:65178532 T / A
gnomAD v4:
chr14-65178532-T-A
Linked Data - NCBI & NCI
dbSNP:
7158173
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.65178532T>A , CM000676.2:g.65178532T>A
GRCh38
NC_000014.8:g.65645250T>A , CM000676.1:g.65645250T>A
GRCh37
NC_000014.7:g.64715003T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'