Canonical Allele Identifier: CA363149132

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691744C>T (hg19) ; chr6:g.30723967C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723967C>T , CM000668.2:g.30723967C>T	GRCh38
NC_000006.11:g.30691744C>T , CM000668.1:g.30691744C>T	GRCh37
NC_000006.10:g.30799723C>T	NCBI36
NG_034142.1:g.8767C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.905C>T MANE Select	ENSP00000339001.7:p.Ala302Val
ENST00000680530.1:n.1767C>T
ENST00000681421.1:n.1971C>T
ENST00000681435.1:c.689C>T	ENSP00000506665.1:p.Ala230Val
ENST00000327892.12:c.905C>T	ENSP00000339001.7:p.Ala302Val
ENST00000330914.7:c.689C>T	ENSP00000365578.2:p.Ala230Val
ENST00000396384.1:c.689C>T	ENSP00000379668.1:p.Ala230Val
ENST00000396389.5:c.851C>T	ENSP00000379672.1:p.Ala284Val
NM_001293212.1:c.965C>T	NP_001280141.1:p.Ala322Val
NM_001293213.1:c.370-71C>T	NP_001280142.1:n.370-71C>T
NM_001293214.1:c.773C>T	NP_001280143.1:p.Ala258Val
NM_001293215.1:c.689C>T	NP_001280144.1:p.Ala230Val
NM_001293216.1:c.689C>T	NP_001280145.1:p.Ala230Val
NM_178014.3:c.905C>T	NP_821133.1:p.Ala302Val
NR_120608.1:n.612C>T
NM_178014.4:c.905C>T MANE Select	NP_821133.1:p.Ala302Val
NM_001293212.2:c.965C>T	NP_001280141.1:p.Ala322Val
NM_001293213.2:c.370-71C>T	NP_001280142.1:n.370-71C>T
NM_001293214.2:c.773C>T	NP_001280143.1:p.Ala258Val
NM_001293215.2:c.689C>T	NP_001280144.1:p.Ala230Val
NM_001293216.2:c.689C>T	NP_001280145.1:p.Ala230Val
NR_120608.2:n.461C>T