ClinGen Allele Registry
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Canonical Allele Identifier:
CA563684471
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.157603332del
GRCh37
chr5:g.157030340del
Linked Data - Sequence & Population
gnomAD v2:
5:157030339 CA / C
gnomAD v3:
5:157603331 CA / C
gnomAD v4:
chr5-157603331-CA-C
Joint Max Group AF
0.00006288 (AFR)
Genomes Max Group AF
0.00006288 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1382639798
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.157603334del , CM000667.2:g.157603334del
GRCh38
NC_000005.9:g.157030342del , CM000667.1:g.157030342del
GRCh37
NC_000005.8:g.156962920del
NCBI36
Search 100 bp 5'
Search 100 bp 3'