Canonical Allele Identifier: CA449776664

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691652C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723875C>G , CM000668.2:g.30723875C>G	GRCh38
NC_000006.11:g.30691652C>G , CM000668.1:g.30691652C>G	GRCh37
NC_000006.10:g.30799631C>G	NCBI36
NG_034142.1:g.8675C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.813C>G MANE Select	ENSP00000339001.7:p.Ala271=
ENST00000680530.1:n.1675C>G
ENST00000681421.1:n.1879C>G
ENST00000681435.1:c.597C>G	ENSP00000506665.1:p.Ala199=
ENST00000327892.12:c.813C>G	ENSP00000339001.7:p.Ala271=
ENST00000330914.7:c.597C>G	ENSP00000365578.2:p.Ala199=
ENST00000396384.1:c.597C>G	ENSP00000379668.1:p.Ala199=
ENST00000396389.5:c.759C>G	ENSP00000379672.1:p.Ala253=
NM_001293212.1:c.873C>G	NP_001280141.1:p.Ala291=
NM_001293213.1:c.370-163C>G	NP_001280142.1:n.370-163C>G
NM_001293214.1:c.681C>G	NP_001280143.1:p.Ala227=
NM_001293215.1:c.597C>G	NP_001280144.1:p.Ala199=
NM_001293216.1:c.597C>G	NP_001280145.1:p.Ala199=
NM_178014.3:c.813C>G	NP_821133.1:p.Ala271=
NR_120608.1:n.584-64C>G
NM_178014.4:c.813C>G MANE Select	NP_821133.1:p.Ala271=
NM_001293212.2:c.873C>G	NP_001280141.1:p.Ala291=
NM_001293213.2:c.370-163C>G	NP_001280142.1:n.370-163C>G
NM_001293214.2:c.681C>G	NP_001280143.1:p.Ala227=
NM_001293215.2:c.597C>G	NP_001280144.1:p.Ala199=
NM_001293216.2:c.597C>G	NP_001280145.1:p.Ala199=
NR_120608.2:n.433-64C>G