Canonical Allele Identifier: CA16603158
Gene: TUBB HGNC NCBI

Linked Data

ClinVar Variation Id: 376764
ClinVar RCV Id: RCV000424756
dbSNP Id: rs1057520046

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30723595C>G , CM000668.2:g.30723595C>G GRCh38
NC_000006.11:g.30691372C>G , CM000668.1:g.30691372C>G GRCh37
NC_000006.10:g.30799351C>G NCBI36
NG_034142.1:g.8395C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000327892.13:c.533C>G MANE Select ENSP00000339001.7:p.Thr178Ser
ENST00000680530.1:n.1395C>G
ENST00000681421.1:n.1599C>G
ENST00000681435.1:c.317C>G ENSP00000506665.1:p.Thr106Ser
ENST00000327892.12:c.533C>G ENSP00000339001.7:p.Thr178Ser
ENST00000330914.7:c.317C>G ENSP00000365578.2:p.Thr106Ser
ENST00000396384.1:c.317C>G ENSP00000379668.1:p.Thr106Ser
ENST00000396389.5:c.479C>G ENSP00000379672.1:p.Thr160Ser
NM_001293212.1:c.593C>G NP_001280141.1:p.Thr198Ser
NM_001293213.1:c.369+164C>G NP_001280142.1:n.369+164C>G
NM_001293214.1:c.401C>G NP_001280143.1:p.Thr134Ser
NM_001293215.1:c.317C>G NP_001280144.1:p.Thr106Ser
NM_001293216.1:c.317C>G NP_001280145.1:p.Thr106Ser
NM_178014.3:c.533C>G NP_821133.1:p.Thr178Ser
NR_120608.1:n.584-344C>G
NM_178014.4:c.533C>G MANE Select NP_821133.1:p.Thr178Ser
NM_001293212.2:c.593C>G NP_001280141.1:p.Thr198Ser
NM_001293213.2:c.369+164C>G NP_001280142.1:n.369+164C>G
NM_001293214.2:c.401C>G NP_001280143.1:p.Thr134Ser
NM_001293215.2:c.317C>G NP_001280144.1:p.Thr106Ser
NM_001293216.2:c.317C>G NP_001280145.1:p.Thr106Ser
NR_120608.2:n.433-344C>G