ClinGen Allele Registry
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Canonical Allele Identifier:
CA890355512
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.163063897del
GRCh37
chr1:g.163033687del
Linked Data - Sequence & Population
gnomAD v3:
1:163063896 GC / G
gnomAD v4:
chr1-163063896-GC-G
Joint Max Group AF
0.00015691 (EAS)
Genomes Max Group AF
0.00015691 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1156547332
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.163063902del , CM000663.2:g.163063902del
GRCh38
NC_000001.10:g.163033692del , CM000663.1:g.163033692del
GRCh37
NC_000001.9:g.161300316del
NCBI36
NG_023312.1:g.297del
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