Canonical Allele Identifier: CA363149230

Gene: TUBB

Linked Data

• ClinVar Variation Id: 1339905
• ClinVar RCV Id: RCV001825288 ; RCV003235602
• dbSNP Id: rs2127749740
• MyVariant Identifiers: chr6:g.30691756G>C (hg19) ; chr6:g.30723979G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723979G>C , CM000668.2:g.30723979G>C	GRCh38
NC_000006.11:g.30691756G>C , CM000668.1:g.30691756G>C	GRCh37
NC_000006.10:g.30799735G>C	NCBI36
NG_034142.1:g.8779G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.917G>C MANE Select	ENSP00000339001.7:p.Arg306Pro
ENST00000680530.1:n.1779G>C
ENST00000681421.1:n.1983G>C
ENST00000681435.1:c.701G>C	ENSP00000506665.1:p.Arg234Pro
ENST00000327892.12:c.917G>C	ENSP00000339001.7:p.Arg306Pro
ENST00000330914.7:c.701G>C	ENSP00000365578.2:p.Arg234Pro
ENST00000396384.1:c.701G>C	ENSP00000379668.1:p.Arg234Pro
ENST00000396389.5:c.863G>C	ENSP00000379672.1:p.Arg288Pro
NM_001293212.1:c.977G>C	NP_001280141.1:p.Arg326Pro
NM_001293213.1:c.370-59G>C	NP_001280142.1:n.370-59G>C
NM_001293214.1:c.785G>C	NP_001280143.1:p.Arg262Pro
NM_001293215.1:c.701G>C	NP_001280144.1:p.Arg234Pro
NM_001293216.1:c.701G>C	NP_001280145.1:p.Arg234Pro
NM_178014.3:c.917G>C	NP_821133.1:p.Arg306Pro
NR_120608.1:n.624G>C
NM_178014.4:c.917G>C MANE Select	NP_821133.1:p.Arg306Pro
NM_001293212.2:c.977G>C	NP_001280141.1:p.Arg326Pro
NM_001293213.2:c.370-59G>C	NP_001280142.1:n.370-59G>C
NM_001293214.2:c.785G>C	NP_001280143.1:p.Arg262Pro
NM_001293215.2:c.701G>C	NP_001280144.1:p.Arg234Pro
NM_001293216.2:c.701G>C	NP_001280145.1:p.Arg234Pro
NR_120608.2:n.473G>C