ClinGen Allele Registry
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Canonical Allele Identifier:
CA637004830
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr21:g.14472787_14472789del
GRCh37
chr21:g.15845108_15845110del
Linked Data - Sequence & Population
gnomAD v2:
21:15845107 TTAA / T
gnomAD v3:
21:14472786 TTAA / T
gnomAD v4:
chr21-14472786-TTAA-T
Linked Data - NCBI & NCI
dbSNP:
1156331241
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.14472795_14472797del , CM000683.2:g.14472795_14472797del
GRCh38
NC_000021.8:g.15845116_15845118del , CM000683.1:g.15845116_15845118del
GRCh37
NC_000021.7:g.14766987_14766989del
NCBI36
Search 100 bp 5'
Search 100 bp 3'