ClinGen Allele Registry
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Canonical Allele Identifier:
CA849569762
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.19970359_19970361del
GRCh37
chr8:g.19827870_19827872del
Linked Data - Sequence & Population
gnomAD v3:
8:19970358 GTCC / G
gnomAD v4:
chr8-19970358-GTCC-G
Joint Max Group AF
0.00002263 (AMR)
Genomes Max Group AF
0.00002263 (AMR)
Linked Data - NCBI & NCI
dbSNP:
1332842949
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.19970363_19970365del , CM000670.2:g.19970363_19970365del
GRCh38
NC_000008.10:g.19827874_19827876del , CM000670.1:g.19827874_19827876del
GRCh37
NC_000008.9:g.19872154_19872156del
NCBI36
Search 100 bp 5'
Search 100 bp 3'