ClinGen Allele Registry
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Canonical Allele Identifier:
CA810627019
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.40415007del
GRCh37
chr5:g.40415109del
Linked Data - Sequence & Population
gnomAD v3:
5:40415006 TA / T
gnomAD v4:
chr5-40415006-TA-T
Linked Data - NCBI & NCI
dbSNP:
1171944806
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.40415007del , CM000667.2:g.40415007del
GRCh38
NC_000005.9:g.40415109del , CM000667.1:g.40415109del
GRCh37
NC_000005.8:g.40450866del
NCBI36
Search 100 bp 5'
Search 100 bp 3'