Canonical Allele Identifier: CA212237667
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 1211170
ClinVar RCV Id: RCV001587648
dbSNP Id: rs373586559
gnomAD v2: 10-104263582-C-A
gnomAD v3: 10-102503825-C-A
gnomAD v4: 10-102503825-C-A
MyVariant Identifiers: chr10:g.104263582C>A (hg19) chr10:g.102503825C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102503825C>A , CM000672.2:g.102503825C>A GRCh38
NC_000010.10:g.104263582C>A , CM000672.1:g.104263582C>A GRCh37
NC_000010.9:g.104253572C>A NCBI36
NG_011901.1:g.3931G>T
NG_021338.1:g.4864C>A , LRG_521:g.4864C>A

Transcript Alleles

HGVS Amino-acid Change
XM_011539859.1:c.-29-299C>A XP_011538161.1:n.-29-299C>A
XM_011539863.1:c.8+839C>A XP_011538165.1:n.8+839C>A
XM_011539863.3:c.8+839C>A XP_011538165.1:n.8+839C>A
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