Canonical Allele Identifier: CA212237648
Gene: SUFU HGNC NCBI

Linked Data

dbSNP Id: rs903460555
MyVariant Identifiers: chr10:g.104263516G>A (hg19) chr10:g.102503759G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102503759G>A , CM000672.2:g.102503759G>A GRCh38
NC_000010.10:g.104263516G>A , CM000672.1:g.104263516G>A GRCh37
NC_000010.9:g.104253506G>A NCBI36
NG_011901.1:g.3997C>T
NG_021338.1:g.4798G>A , LRG_521:g.4798G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011539859.1:c.-29-365G>A XP_011538161.1:n.-29-365G>A
XM_011539863.1:c.8+773G>A XP_011538165.1:n.8+773G>A
XM_011539863.3:c.8+773G>A XP_011538165.1:n.8+773G>A
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