ClinGen Allele Registry
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Canonical Allele Identifier:
CA747163335
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr21:g.14472605_14472610del
GRCh37
chr21:g.15844926_15844931del
Linked Data - NCBI & NCI
dbSNP:
1398830786
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.14472606_14472611del , CM000683.2:g.14472606_14472611del
GRCh38
NC_000021.8:g.15844927_15844932del , CM000683.1:g.15844927_15844932del
GRCh37
NC_000021.7:g.14766798_14766803del
NCBI36
Search 100 bp 5'
Search 100 bp 3'