Canonical Allele Identifier: CA391685348
Gene: BUB1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40185639T>C , CM000677.2:g.40185639T>C GRCh38
NC_000015.9:g.40477840T>C , CM000677.1:g.40477840T>C GRCh37
NC_000015.8:g.38265132T>C NCBI36
NG_016338.1:g.29631T>C , LRG_489:g.29631T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000287598.11:c.1055T>C MANE Select ENSP00000287598.7:p.Val352Ala
ENST00000287598.10:c.1055T>C ENSP00000287598.6:p.Val352Ala
ENST00000412359.7:c.1097T>C ENSP00000398470.3:p.Val366Ala
ENST00000557848.1:n.314T>C
ENST00000559733.5:c.170+1756T>C
ENST00000559772.1:n.168T>C
NM_001211.5:c.1055T>C , LRG_489t1:c.1055T>C NP_001202.4:p.Val352Ala
XR_001751506.1:n.218-5438A>G
NM_001211.6:c.1055T>C MANE Select NP_001202.5:p.Val352Ala