Canonical Allele Identifier: CA391685319
Gene: BUB1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40185633A>C , CM000677.2:g.40185633A>C GRCh38
NC_000015.9:g.40477834A>C , CM000677.1:g.40477834A>C GRCh37
NC_000015.8:g.38265126A>C NCBI36
NG_016338.1:g.29625A>C , LRG_489:g.29625A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000287598.11:c.1049A>C MANE Select ENSP00000287598.7:p.Gln350Pro
ENST00000287598.10:c.1049A>C ENSP00000287598.6:p.Gln350Pro
ENST00000412359.7:c.1091A>C ENSP00000398470.3:p.Gln364Pro
ENST00000557848.1:n.308A>C
ENST00000559733.5:c.170+1750A>C
ENST00000559772.1:n.162A>C
NM_001211.5:c.1049A>C , LRG_489t1:c.1049A>C NP_001202.4:p.Gln350Pro
XR_001751506.1:n.218-5432T>G
NM_001211.6:c.1049A>C MANE Select NP_001202.5:p.Gln350Pro