ClinGen Allele Registry
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Canonical Allele Identifier:
CA553104062
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.99353052del
GRCh37
chr4:g.100274209del
Linked Data - Sequence & Population
gnomAD v2:
4:100274208 TC / T
Linked Data - NCBI & NCI
dbSNP:
1480222321
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.99353054del , CM000666.2:g.99353054del
GRCh38
NC_000004.11:g.100274211del , CM000666.1:g.100274211del
GRCh37
NC_000004.10:g.100493234del
NCBI36
NG_011718.1:g.4709del
Search 100 bp 5'
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