Canonical Allele Identifier: CA449776858
Gene: TUBB HGNC NCBI

Linked Data

dbSNP Id: rs1562158511
MyVariant Identifiers: chr6:g.30691772C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30723995C>T , CM000668.2:g.30723995C>T GRCh38
NC_000006.11:g.30691772C>T , CM000668.1:g.30691772C>T GRCh37
NC_000006.10:g.30799751C>T NCBI36
NG_034142.1:g.8795C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000327892.13:c.933C>T MANE Select ENSP00000339001.7:p.Leu311=
ENST00000680530.1:n.1795C>T
ENST00000681421.1:n.1999C>T
ENST00000681435.1:c.717C>T ENSP00000506665.1:p.Leu239=
ENST00000327892.12:c.933C>T ENSP00000339001.7:p.Leu311=
ENST00000330914.7:c.717C>T ENSP00000365578.2:p.Leu239=
ENST00000396384.1:c.717C>T ENSP00000379668.1:p.Leu239=
ENST00000396389.5:c.879C>T ENSP00000379672.1:p.Leu293=
NM_001293212.1:c.993C>T NP_001280141.1:p.Leu331=
NM_001293213.1:c.370-43C>T NP_001280142.1:n.370-43C>T
NM_001293214.1:c.801C>T NP_001280143.1:p.Leu267=
NM_001293215.1:c.717C>T NP_001280144.1:p.Leu239=
NM_001293216.1:c.717C>T NP_001280145.1:p.Leu239=
NM_178014.3:c.933C>T NP_821133.1:p.Leu311=
NR_120608.1:n.640C>T
NM_178014.4:c.933C>T MANE Select NP_821133.1:p.Leu311=
NM_001293212.2:c.993C>T NP_001280141.1:p.Leu331=
NM_001293213.2:c.370-43C>T NP_001280142.1:n.370-43C>T
NM_001293214.2:c.801C>T NP_001280143.1:p.Leu267=
NM_001293215.2:c.717C>T NP_001280144.1:p.Leu239=
NM_001293216.2:c.717C>T NP_001280145.1:p.Leu239=
NR_120608.2:n.489C>T