Canonical Allele Identifier: CA1810127777

Gene: SYBU

Linked Data

• dbSNP Id: rs3133926

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.109677149A>C , CM000670.2:g.109677149A>C	GRCh38
NC_000008.10:g.110689378A>C , CM000670.1:g.110689378A>C	GRCh37
NC_000008.9:g.110758554A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000408889.7:c.-129+3562T>G	ENSP00000386196.3:n.-129+3562T>G
ENST00000422135.5:c.-58+14184T>G	ENSP00000407118.1:n.-58+14184T>G
ENST00000527600.5:c.-221+3562T>G	ENSP00000434612.1:n.-221+3562T>G
ENST00000527664.1:n.164+3562T>G
ENST00000528716.5:c.-179+3562T>G	ENSP00000436520.1:n.-179+3562T>G
ENST00000529190.5:c.-58+14184T>G	ENSP00000432835.1:n.-58+14184T>G
ENST00000531230.5:c.-210+3562T>G	ENSP00000434158.1:n.-210+3562T>G
ENST00000532189.5:c.-129+3562T>G	ENSP00000436908.1:n.-129+3562T>G
ENST00000532779.5:c.25+14184T>G	ENSP00000436266.1:n.25+14184T>G
ENST00000533171.5:c.-58+3562T>G	ENSP00000434679.1:n.-58+3562T>G
ENST00000533821.5:c.-58+3041T>G	ENSP00000431469.1:n.-58+3041T>G
ENST00000534184.5:c.-58+3562T>G	ENSP00000432291.1:n.-58+3562T>G
ENST00000534578.5:c.-58+14184T>G	ENSP00000431895.1:n.-58+14184T>G
NM_001099743.1:c.-58+14184T>G	NP_001093213.1:n.-58+14184T>G
NM_001099744.1:c.-58+14184T>G	NP_001093214.1:n.-58+14184T>G
NM_001099745.1:c.-58+3562T>G	NP_001093215.1:n.-58+3562T>G
NM_001099746.1:c.-129+3562T>G	NP_001093216.1:n.-129+3562T>G
XM_017013615.1:c.-210+3562T>G	XP_016869104.1:n.-210+3562T>G
NM_001099743.2:c.-58+14184T>G	NP_001093213.1:n.-58+14184T>G
NM_001099745.2:c.-58+3562T>G	NP_001093215.1:n.-58+3562T>G
NM_001099744.2:c.-58+14184T>G	NP_001093214.1:n.-58+14184T>G
NM_001099746.2:c.-129+3562T>G	NP_001093216.1:n.-129+3562T>G