ClinGen Allele Registry
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Canonical Allele Identifier:
CA601216151
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.102845217del
GRCh37
chr11:g.102715948del
Linked Data - Sequence & Population
gnomAD v2:
11:102715947 GA / G
gnomAD v3:
11:102845216 GA / G
gnomAD v4:
chr11-102845216-GA-G
Linked Data - NCBI & NCI
dbSNP:
35068180
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.102845221del , CM000673.2:g.102845221del
GRCh38
NC_000011.9:g.102715952del , CM000673.1:g.102715952del
GRCh37
NC_000011.8:g.102221162del
NCBI36
NG_012100.1:g.3395del
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