Canonical Allele Identifier: CA212237712
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 1196268
ClinVar RCV Id: RCV001559682
dbSNP Id: rs186314614
gnomAD v2: 10-104263630-G-A
gnomAD v3: 10-102503873-G-A
gnomAD v4: 10-102503873-G-A
MyVariant Identifiers: chr10:g.104263630G>A (hg19) chr10:g.102503873G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102503873G>A , CM000672.2:g.102503873G>A GRCh38
NC_000010.10:g.104263630G>A , CM000672.1:g.104263630G>A GRCh37
NC_000010.9:g.104253620G>A NCBI36
NG_011901.1:g.3883C>T
NG_021338.1:g.4912G>A , LRG_521:g.4912G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011539859.1:c.-29-251G>A XP_011538161.1:n.-29-251G>A
XM_011539863.1:c.8+887G>A XP_011538165.1:n.8+887G>A
XM_011539863.3:c.8+887G>A XP_011538165.1:n.8+887G>A
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