ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA13963225
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.69034335G>T
GRCh37
chr14:g.69501052G>T
Linked Data - Sequence & Population
gnomAD v2:
14:69501052 G / T
gnomAD v3:
14:69034335 G / T
gnomAD v4:
chr14-69034335-G-T
Joint Max Group AF
0.95522013 (EAS)
Genomes Max Group AF
0.95522013 (EAS)
Linked Data - NCBI & NCI
dbSNP:
761899
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.69034335G>T , CM000676.2:g.69034335G>T
GRCh38
NC_000014.8:g.69501052G>T , CM000676.1:g.69501052G>T
GRCh37
NC_000014.7:g.68570805G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'