Canonical Allele Identifier: CA391685327
Gene: BUB1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40185634G>T , CM000677.2:g.40185634G>T GRCh38
NC_000015.9:g.40477835G>T , CM000677.1:g.40477835G>T GRCh37
NC_000015.8:g.38265127G>T NCBI36
NG_016338.1:g.29626G>T , LRG_489:g.29626G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000287598.11:c.1050G>T MANE Select ENSP00000287598.7:p.Gln350His
ENST00000287598.10:c.1050G>T ENSP00000287598.6:p.Gln350His
ENST00000412359.7:c.1092G>T ENSP00000398470.3:p.Gln364His
ENST00000557848.1:n.309G>T
ENST00000559733.5:c.170+1751G>T
ENST00000559772.1:n.163G>T
NM_001211.5:c.1050G>T , LRG_489t1:c.1050G>T NP_001202.4:p.Gln350His
XR_001751506.1:n.218-5433C>A
NM_001211.6:c.1050G>T MANE Select NP_001202.5:p.Gln350His