Canonical Allele Identifier: CA391685354
Gene: BUB1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40185641A>G , CM000677.2:g.40185641A>G GRCh38
NC_000015.9:g.40477842A>G , CM000677.1:g.40477842A>G GRCh37
NC_000015.8:g.38265134A>G NCBI36
NG_016338.1:g.29633A>G , LRG_489:g.29633A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000287598.11:c.1057A>G MANE Select ENSP00000287598.7:p.Met353Val
ENST00000287598.10:c.1057A>G ENSP00000287598.6:p.Met353Val
ENST00000412359.7:c.1099A>G ENSP00000398470.3:p.Met367Val
ENST00000557848.1:n.316A>G
ENST00000559733.5:c.170+1758A>G
ENST00000559772.1:n.170A>G
NM_001211.5:c.1057A>G , LRG_489t1:c.1057A>G NP_001202.4:p.Met353Val
XR_001751506.1:n.218-5440T>C
NM_001211.6:c.1057A>G MANE Select NP_001202.5:p.Met353Val