ClinGen Allele Registry
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Canonical Allele Identifier:
CA747163372
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr21:g.14472684_14472685del
GRCh37
chr21:g.15845005_15845006del
Linked Data - Sequence & Population
gnomAD v3:
21:14472683 TAA / T
gnomAD v4:
chr21-14472683-TAA-T
Linked Data - NCBI & NCI
dbSNP:
1425232144
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.14472684_14472685del , CM000683.2:g.14472684_14472685del
GRCh38
NC_000021.8:g.15845005_15845006del , CM000683.1:g.15845005_15845006del
GRCh37
NC_000021.7:g.14766876_14766877del
NCBI36
Search 100 bp 5'
Search 100 bp 3'