Canonical Allele Identifier: CA212237694
Gene: SUFU HGNC NCBI

Linked Data

dbSNP Id: rs534182860
gnomAD v3: 10-102503853-T-C
gnomAD v4: 10-102503853-T-C
MyVariant Identifiers: chr10:g.104263610T>C (hg19) chr10:g.102503853T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102503853T>C , CM000672.2:g.102503853T>C GRCh38
NC_000010.10:g.104263610T>C , CM000672.1:g.104263610T>C GRCh37
NC_000010.9:g.104253600T>C NCBI36
NG_011901.1:g.3903A>G
NG_021338.1:g.4892T>C , LRG_521:g.4892T>C

Transcript Alleles

HGVS Amino-acid Change
XM_011539859.1:c.-29-271T>C XP_011538161.1:n.-29-271T>C
XM_011539863.1:c.8+867T>C XP_011538165.1:n.8+867T>C
XM_011539863.3:c.8+867T>C XP_011538165.1:n.8+867T>C
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