Canonical Allele Identifier: CA212237692
Gene: SUFU HGNC NCBI

Linked Data

dbSNP Id: rs765510860
gnomAD v3: 10-102503831-AG-A
gnomAD v4: 10-102503831-AG-A
MyVariant Identifiers: chr10:g.104263589del (hg19) chr10:g.102503832del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102503834del , CM000672.2:g.102503834del GRCh38
NC_000010.10:g.104263591del , CM000672.1:g.104263591del GRCh37
NC_000010.9:g.104253581del NCBI36
NG_011901.1:g.3924del
NG_021338.1:g.4873del , LRG_521:g.4873del

Transcript Alleles

HGVS Amino-acid Change
XM_011539859.1:c.-29-290del XP_011538161.1:n.-29-290del
XM_011539863.1:c.8+848del XP_011538165.1:n.8+848del
XM_011539863.3:c.8+848del XP_011538165.1:n.8+848del
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