Canonical Allele Identifier: CA7475638
Gene: BUB1B HGNC NCBI

Linked Data

dbSNP Id: rs200788206

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40185632C>G , CM000677.2:g.40185632C>G GRCh38
NC_000015.9:g.40477833C>G , CM000677.1:g.40477833C>G GRCh37
NC_000015.8:g.38265125C>G NCBI36
NG_016338.1:g.29624C>G , LRG_489:g.29624C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000287598.11:c.1048C>G MANE Select ENSP00000287598.7:p.Gln350Glu
ENST00000287598.10:c.1048C>G ENSP00000287598.6:p.Gln350Glu
ENST00000412359.7:c.1090C>G ENSP00000398470.3:p.Gln364Glu
ENST00000557848.1:n.307C>G
ENST00000559733.5:c.170+1749C>G
ENST00000559772.1:n.161C>G
NM_001211.5:c.1048C>G , LRG_489t1:c.1048C>G NP_001202.4:p.Gln350Glu
XR_001751506.1:n.218-5431G>C
NM_001211.6:c.1048C>G MANE Select NP_001202.5:p.Gln350Glu