Canonical Allele Identifier: CA489706784
Gene: BUB1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.40477838A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40185637A>C , CM000677.2:g.40185637A>C GRCh38
NC_000015.9:g.40477838A>C , CM000677.1:g.40477838A>C GRCh37
NC_000015.8:g.38265130A>C NCBI36
NG_016338.1:g.29629A>C , LRG_489:g.29629A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000287598.11:c.1053A>C MANE Select ENSP00000287598.7:p.Pro351=
ENST00000287598.10:c.1053A>C ENSP00000287598.6:p.Pro351=
ENST00000412359.7:c.1095A>C ENSP00000398470.3:p.Pro365=
ENST00000557848.1:n.312A>C
ENST00000559733.5:c.170+1754A>C
ENST00000559772.1:n.166A>C
NM_001211.5:c.1053A>C , LRG_489t1:c.1053A>C NP_001202.4:p.Pro351=
XR_001751506.1:n.218-5436T>G
NM_001211.6:c.1053A>C MANE Select NP_001202.5:p.Pro351=