Canonical Allele Identifier: CA659051772
Gene: SUFU HGNC NCBI

Linked Data

dbSNP Id: rs1342374033
gnomAD v3: 10-102503829-A-G
gnomAD v4: 10-102503829-A-G
MyVariant Identifiers: chr10:g.104263586A>G (hg19) chr10:g.102503829A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102503829A>G , CM000672.2:g.102503829A>G GRCh38
NC_000010.10:g.104263586A>G , CM000672.1:g.104263586A>G GRCh37
NC_000010.9:g.104253576A>G NCBI36
NG_011901.1:g.3927T>C
NG_021338.1:g.4868A>G , LRG_521:g.4868A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011539859.1:c.-29-295A>G XP_011538161.1:n.-29-295A>G
XM_011539863.1:c.8+843A>G XP_011538165.1:n.8+843A>G
XM_011539863.3:c.8+843A>G XP_011538165.1:n.8+843A>G
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