ClinGen Allele Registry
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Canonical Allele Identifier:
CA783226036
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.1106926_1106937del
GRCh37
chr19:g.1106925_1106936del
Linked Data - Sequence & Population
gnomAD v3:
19:1106925 TGTGCTGGCTGCA / T
gnomAD v4:
chr19-1106925-TGTGCTGGCTGCA-T
Joint Max Group AF
0.00000624 (AFR)
Genomes Max Group AF
0.000008 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1329170863
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.1106933_1106944del , CM000681.2:g.1106933_1106944del
GRCh38
NC_000019.9:g.1106932_1106943del , CM000681.1:g.1106932_1106943del
GRCh37
NC_000019.8:g.1057932_1057943del
NCBI36
NG_050621.1:g.8008_8019del
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