Canonical Allele Identifier: CA659051738
Gene: SUFU HGNC NCBI

Linked Data

dbSNP Id: rs1449301390
MyVariant Identifiers: chr10:g.104263503C>T (hg19) chr10:g.102503746C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102503746C>T , CM000672.2:g.102503746C>T GRCh38
NC_000010.10:g.104263503C>T , CM000672.1:g.104263503C>T GRCh37
NC_000010.9:g.104253493C>T NCBI36
NG_011901.1:g.4010G>A
NG_021338.1:g.4785C>T , LRG_521:g.4785C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011539859.1:c.-29-378C>T XP_011538161.1:n.-29-378C>T
XM_011539863.1:c.8+760C>T XP_011538165.1:n.8+760C>T
XM_011539863.3:c.8+760C>T XP_011538165.1:n.8+760C>T
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