ClinGen Allele Registry
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Canonical Allele Identifier:
CA747163411
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr21:g.14472769_14472770insT
GRCh37
chr21:g.15845090_15845091insT
Linked Data - Sequence & Population
gnomAD v3:
21:14472769 C / CT
gnomAD v4:
chr21-14472769-C-CT
Linked Data - NCBI & NCI
dbSNP:
1402322349
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.14472771dup , CM000683.2:g.14472771dup
GRCh38
NC_000021.8:g.15845092dup , CM000683.1:g.15845092dup
GRCh37
NC_000021.7:g.14766963dup
NCBI36
Search 100 bp 5'
Search 100 bp 3'