Canonical Allele Identifier: CA489706781
Gene: BUB1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.40477832A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40185631A>G , CM000677.2:g.40185631A>G GRCh38
NC_000015.9:g.40477832A>G , CM000677.1:g.40477832A>G GRCh37
NC_000015.8:g.38265124A>G NCBI36
NG_016338.1:g.29623A>G , LRG_489:g.29623A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000287598.11:c.1047A>G MANE Select ENSP00000287598.7:p.Arg349=
ENST00000287598.10:c.1047A>G ENSP00000287598.6:p.Arg349=
ENST00000412359.7:c.1089A>G ENSP00000398470.3:p.Arg363=
ENST00000557848.1:n.306A>G
ENST00000559733.5:c.170+1748A>G
ENST00000559772.1:n.160A>G
NM_001211.5:c.1047A>G , LRG_489t1:c.1047A>G NP_001202.4:p.Gln349=
XR_001751506.1:n.218-5430T>C
NM_001211.6:c.1047A>G MANE Select NP_001202.5:p.Arg349=