Canonical Allele Identifier: CA449561882

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691064T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723287T>G , CM000668.2:g.30723287T>G	GRCh38
NC_000006.11:g.30691064T>G , CM000668.1:g.30691064T>G	GRCh37
NC_000006.10:g.30799043T>G	NCBI36
NG_034142.1:g.8087T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000327892.13:c.278-53T>G MANE Select	ENSP00000339001.7:n.278-53T>G
ENST00000680530.1:n.1140-53T>G
ENST00000681421.1:n.1344-53T>G
ENST00000681435.1:c.62-53T>G	ENSP00000506665.1:n.62-53T>G
ENST00000327892.12:c.278-53T>G	ENSP00000339001.7:n.278-53T>G
ENST00000330914.7:c.62-53T>G	ENSP00000365578.2:n.62-53T>G
ENST00000396384.1:c.62-53T>G	ENSP00000379668.1:n.62-53T>G
ENST00000396389.5:c.224-53T>G	ENSP00000379672.1:n.224-53T>G
NM_001293212.1:c.338-53T>G	NP_001280141.1:n.338-53T>G
NM_001293213.1:c.278-53T>G	NP_001280142.1:n.278-53T>G
NM_001293214.1:c.146-53T>G	NP_001280143.1:n.146-53T>G
NM_001293215.1:c.62-53T>G	NP_001280144.1:n.62-53T>G
NM_001293216.1:c.62-53T>G	NP_001280145.1:n.62-53T>G
NM_178014.3:c.278-53T>G	NP_821133.1:n.278-53T>G
NR_120608.1:n.583+259T>G
NM_178014.4:c.278-53T>G MANE Select	NP_821133.1:n.278-53T>G
NM_001293212.2:c.338-53T>G	NP_001280141.1:n.338-53T>G
NM_001293213.2:c.278-53T>G	NP_001280142.1:n.278-53T>G
NM_001293214.2:c.146-53T>G	NP_001280143.1:n.146-53T>G
NM_001293215.2:c.62-53T>G	NP_001280144.1:n.62-53T>G
NM_001293216.2:c.62-53T>G	NP_001280145.1:n.62-53T>G
NR_120608.2:n.432+259T>G