Canonical Allele Identifier: CA489706789
Gene: BUB1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.40477841T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40185640T>G , CM000677.2:g.40185640T>G GRCh38
NC_000015.9:g.40477841T>G , CM000677.1:g.40477841T>G GRCh37
NC_000015.8:g.38265133T>G NCBI36
NG_016338.1:g.29632T>G , LRG_489:g.29632T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000287598.11:c.1056T>G MANE Select ENSP00000287598.7:p.Val352=
ENST00000287598.10:c.1056T>G ENSP00000287598.6:p.Val352=
ENST00000412359.7:c.1098T>G ENSP00000398470.3:p.Val366=
ENST00000557848.1:n.315T>G
ENST00000559733.5:c.170+1757T>G
ENST00000559772.1:n.169T>G
NM_001211.5:c.1056T>G , LRG_489t1:c.1056T>G NP_001202.4:p.Val352=
XR_001751506.1:n.218-5439A>C
NM_001211.6:c.1056T>G MANE Select NP_001202.5:p.Val352=