ClinGen Allele Registry
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Canonical Allele Identifier:
CA637004828
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr21:g.14472756_14472761del
GRCh37
chr21:g.15845077_15845082del
Linked Data - Sequence & Population
gnomAD v2:
21:15845076 AGTGCTT / A
gnomAD v3:
21:14472755 AGTGCTT / A
gnomAD v4:
chr21-14472755-AGTGCTT-A
Linked Data - NCBI & NCI
dbSNP:
1489837677
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.14472756_14472761del , CM000683.2:g.14472756_14472761del
GRCh38
NC_000021.8:g.15845077_15845082del , CM000683.1:g.15845077_15845082del
GRCh37
NC_000021.7:g.14766948_14766953del
NCBI36
Search 100 bp 5'
Search 100 bp 3'