Canonical Allele Identifier: CA391685344
Gene: BUB1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40185638G>C , CM000677.2:g.40185638G>C GRCh38
NC_000015.9:g.40477839G>C , CM000677.1:g.40477839G>C GRCh37
NC_000015.8:g.38265131G>C NCBI36
NG_016338.1:g.29630G>C , LRG_489:g.29630G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000287598.11:c.1054G>C MANE Select ENSP00000287598.7:p.Val352Leu
ENST00000287598.10:c.1054G>C ENSP00000287598.6:p.Val352Leu
ENST00000412359.7:c.1096G>C ENSP00000398470.3:p.Val366Leu
ENST00000557848.1:n.313G>C
ENST00000559733.5:c.170+1755G>C
ENST00000559772.1:n.167G>C
NM_001211.5:c.1054G>C , LRG_489t1:c.1054G>C NP_001202.4:p.Val352Leu
XR_001751506.1:n.218-5437C>G
NM_001211.6:c.1054G>C MANE Select NP_001202.5:p.Val352Leu